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The STARband® is a patient specific cranial orthosis that redirects the head growth to improve proportion and symmetry. It is intended for use on infants from 3 to 18 months of age, with moderate-to-severe non-synostotic positional head shape deformities, including infants with plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads by applying mild pressure to prominent regions of the infant's cranium in order to improve cranial symmetry and/or shape. This device is also indicated for adjunctive use for infants from 3 to 18 months of age whose synostosis has been surgically corrected, but who still have moderate-to-severe cranial deformities including plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads. The STARband® is made with an outer copolymer plastic shell and an inner liner made of pelite polyethylene foam or Aliplast foam (closed cell polyethylene). It utilizes a side opening design and is held in place by a Velcro® strap across the side opening.
ORTHOMERICA PRODUCTS, INC.
704A
In Commercial Distribution
- B151704A0 ()
704A
- Cranial orthosis
The STARband® Plus is a patient specific cranial orthosis that redirects the head growth to improve proportion and symmetry. It is intended for use on infants from 3 to 18 months of age, with moderate-to-severe non-synostotic positional head shape deformities, including infants with plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads by applying mild pressure to prominent regions of the infant's cranium in order to improve cranial symmetry and/or shape. This device is also indicated for adjunctive use for infants from 3 to 18 months of age whose synostosis has been surgically corrected, but who still have moderate-to-severe cranial deformities including plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads.
ORTHOMERICA PRODUCTS, INC.
704.09PA
In Commercial Distribution
- B15170409PA0 ()
704.09PA
- Cranial orthosis
The STARband® Plus is a patient specific cranial orthosis that redirects the head growth to improve proportion and symmetry. It is intended for use on infants from 3 to 18 months of age, with moderate-to-severe non-synostotic positional head shape deformities, including infants with plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads by applying mild pressure to prominent regions of the infant's cranium in order to improve cranial symmetry and/or shape. This device is also indicated for adjunctive use for infants from 3 to 18 months of age whose synostosis has been surgically corrected, but who still have moderate-to-severe cranial deformities including plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads.
ORTHOMERICA PRODUCTS, INC.
704.09A
In Commercial Distribution
- B15170409A0 ()
704.09A
- Cranial orthosis
The St. Louis Band is a patient specific cranial orthosis that redirects the head growth to improve proportion and symmetry. It is intended for use on infants from 3 to 18 months of age, with moderate-to-severe non-synostotic positional head shape deformities, including infants with plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads by applying mild pressure to prominent regions of the infant's cranium in order to improve cranial symmetry and/or shape. This device is also indicated for adjunctive use for infants from 3 to 18 months of age whose synostosis has been surgically corrected, but who still have moderate-to-severe cranial deformities including plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads. The St. Louis Band is made with an outer copolymer plastic shell and an inner liner made of Aliplast foam (closed cell polyethylene). It utilizes an overlapping bi-valve design with a sliding rivet mechanism and is held in place by a Velcro® strap.
ORTHOMERICA PRODUCTS, INC.
704.08PA
In Commercial Distribution
- B15170408PA0 ()
704.08PA
- Cranial orthosis
The STARlight® PRO is a patient specific cranial orthosis that redirects the head growth to improve proportion and symmetry. It is intended for adjunctive use for infants from 3 to 18 months of age whose synostosis has been surgically corrected, but who still have moderate-to-severe cranial deformities including plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads. The STARlight® PRO is made of clear Surlyn plastic or clear co-polyester plastic and may contain optional Aliplast foam (closed cell polyethylene) padding and/or Reston (polyurethane) foam. It utilizes two side openings and is held in place by a Velcro® straps across the side openings.
ORTHOMERICA PRODUCTS, INC.
704.07PA
In Commercial Distribution
- B15170407PA0 ()
704.07PA
- Cranial orthosis
The STARband® Bi-Valve is a patient specific cranial orthosis that redirects the head growth to improve proportion and symmetry. It is intended for use on infants from 3 to 18 months of age, with moderate-to-severe non-synostotic positional head shape deformities, including infants with plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads by applying mild pressure to prominent regions of the infant's cranium in order to improve cranial symmetry and/or shape. This device is also indicated for adjunctive use for infants from 3 to 18 months of age whose synostosis has been surgically corrected, but who still have moderate-to-severe cranial deformities including plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads. The STARband® Bi-Valve is made with an outer copolymer plastic shell and an inner liner made of pelite polyethylene foam or Aliplast foam (closed cell polyethylene). It utilizes an overlapping bi-valve design with a sliding mechanism and is held in place by a Velcro® strap.
ORTHOMERICA PRODUCTS, INC.
704.06PA
In Commercial Distribution
- B15170406PA0 ()
704.06PA
- Cranial orthosis
The STARband® Bi-Valve is a patient specific cranial orthosis that redirects the head growth to improve proportion and symmetry. It is intended for use on infants from 3 to 18 months of age, with moderate-to-severe non-synostotic positional head shape deformities, including infants with plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads by applying mild pressure to prominent regions of the infant's cranium in order to improve cranial symmetry and/or shape. This device is also indicated for adjunctive use for infants from 3 to 18 months of age whose synostosis has been surgically corrected, but who still have moderate-to-severe cranial deformities including plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads. The STARband® Bi-Valve is made with an outer copolymer plastic shell and an inner liner made of pelite polyethylene foam or Aliplast foam (closed cell polyethylene). It utilizes an overlapping bi-valve design with a sliding mechanism and is held in place by a Velcro® strap.
ORTHOMERICA PRODUCTS, INC.
704.06A
In Commercial Distribution
- B15170406A0 ()
704.06A
- Cranial orthosis
The Clarren Helmet is a patient specific cranial orthosis that applies passive pressure to prominent regions of an infant’s cranium in order to improve cranial symmetry and/or shape in infants from 3 to 18 months of age with moderate to severe nonsynostotic positional plagiocephaly, including infants with plagiocephalic, brachycephalic, and scaphocephalic- shaped heads. The Clarren Helmet is made with an outer polypropylene plastic shell with a Plastizote inner liner and a chinstrap to help hold the helmet in place.
ORTHOMERICA PRODUCTS, INC.
704.05A
In Commercial Distribution
- B15170405A0 ()
704.05A
- Cranial orthosis
The STARlight® is a patient specific cranial orthosis that redirects the head growth to improve proportion and symmetry. It is intended for use on infants from 3 to 18 months of age, with moderate-to-severe non-synostotic positional head shape deformities, including infants with plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads by applying mild pressure to prominent regions of the infant's cranium in order to improve cranial symmetry and/or shape. This device is also indicated for adjunctive use for infants from 3 to 18 months of age whose synostosis has been surgically corrected, but who still have moderate-to-severe cranial deformities including plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads. The STARlight® is made of clear Surlyn plastic or clear co-polyester plastic and may contain optional Aliplast foam (closed cell polyethylene) padding. It utilizes a side opening design and is held in place by a Velcro® strap across the side opening.
ORTHOMERICA PRODUCTS, INC.
704.03PA
In Commercial Distribution
- B15170403PA0 ()
704.03PA
- Cranial orthosis
The STARlight® is a patient specific cranial orthosis that redirects the head growth to improve proportion and symmetry. It is intended for use on infants from 3 to 18 months of age, with moderate-to-severe non-synostotic positional head shape deformities, including infants with plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads by applying mild pressure to prominent regions of the infant's cranium in order to improve cranial symmetry and/or shape. This device is also indicated for adjunctive use for infants from 3 to 18 months of age whose synostosis has been surgically corrected, but who still have moderate-to-severe cranial deformities including plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads. The STARlight® is made of clear Surlyn plastic or clear co-polyester plastic and may contain optional Aliplast foam (closed cell polyethylene) padding. It utilizes a side opening design and is held in place by a Velcro® strap across the side opening.
ORTHOMERICA PRODUCTS, INC.
704.03A
In Commercial Distribution
- B15170403A0 ()
704.03A
- Cranial orthosis
The STARlight® Bi-Valve is a patient specific cranial orthosis that redirects the head growth to improve proportion and symmetry. It is intended for use on infants from 3 to 18 months of age, with moderate-to-severe non-synostotic positional head shape deformities, including infants with plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads by applying mild pressure to prominent regions of the infant's cranium in order to improve cranial symmetry and/or shape. This device is also indicated for adjunctive use for infants from 3 to 18 months of age whose synostosis has been surgically corrected, but who still have moderate-to-severe cranial deformities including plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads. The STARlight® Bi-Valve is made of clear Surlyn plastic or clear co-polyester plastic and may contain optional Aliplast foam (closed cell polyethylene) padding. It utilizes an overlapping bi-valve design with a sliding mechanism and is held in place by a Velcro® strap.
ORTHOMERICA PRODUCTS, INC.
704.01A
In Commercial Distribution
- B15170401A0 ()
704.01A
- Cranial orthosis
The STARband® is a patient specific cranial orthosis that redirects the head growth to improve proportion and symmetry. It is intended for use on infants from 3 to 18 months of age, with moderate-to-severe non-synostotic positional head shape deformities, including infants with plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads by applying mild pressure to prominent regions of the infant's cranium in order to improve cranial symmetry and/or shape. This device is also indicated for adjunctive use for infants from 3 to 18 months of age whose synostosis has been surgically corrected, but who still have moderate-to-severe cranial deformities including plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads. The STARband® is made with an outer copolymer plastic shell and an inner liner made of pelite polyethylene foam or Aliplast foam (closed cell polyethylene). It utilizes a side opening design and is held in place by a Velcro® strap across the side opening.
ORTHOMERICA PRODUCTS, INC.
703PA
In Commercial Distribution
- B151703PA0 ()
703PA
- Cranial orthosis
The STARband® is a patient specific cranial orthosis that redirects the head growth to improve proportion and symmetry. It is intended for use on infants from 3 to 18 months of age, with moderate-to-severe non-synostotic positional head shape deformities, including infants with plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads by applying mild pressure to prominent regions of the infant's cranium in order to improve cranial symmetry and/or shape. This device is also indicated for adjunctive use for infants from 3 to 18 months of age whose synostosis has been surgically corrected, but who still have moderate-to-severe cranial deformities including plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads. The STARband® is made with an outer copolymer plastic shell and an inner liner made of pelite polyethylene foam or Aliplast foam (closed cell polyethylene). It utilizes a side opening design and is held in place by a Velcro® strap across the side opening.
ORTHOMERICA PRODUCTS, INC.
703A
In Commercial Distribution
- B151703A0 ()
703A
- Cranial orthosis
The STARband® Plus is a patient specific cranial orthosis that redirects the head growth to improve proportion and symmetry. It is intended for use on infants from 3 to 18 months of age, with moderate-to-severe non-synostotic positional head shape deformities, including infants with plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads by applying mild pressure to prominent regions of the infant's cranium in order to improve cranial symmetry and/or shape. This device is also indicated for adjunctive use for infants from 3 to 18 months of age whose synostosis has been surgically corrected, but who still have moderate-to-severe cranial deformities including plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads.
ORTHOMERICA PRODUCTS, INC.
703.09A
In Commercial Distribution
- B15170309A0 ()
703.09A
- Cranial orthosis
The STARlight® PRO is a patient specific cranial orthosis that redirects the head growth to improve proportion and symmetry. It is intended for adjunctive use for infants from 3 to 18 months of age whose synostosis has been surgically corrected, but who still have moderate-to-severe cranial deformities including plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads. The STARlight® PRO is made of clear Surlyn plastic or clear co-polyester plastic and may contain optional Aliplast foam (closed cell polyethylene) padding and/or Reston (polyurethane) foam. It utilizes two side openings and is held in place by a Velcro® straps across the side openings.
ORTHOMERICA PRODUCTS, INC.
703.07PA
In Commercial Distribution
- B15170307PA0 ()
703.07PA
- Cranial orthosis
The STARband® Bi-Valve is a patient specific cranial orthosis that redirects the head growth to improve proportion and symmetry. It is intended for use on infants from 3 to 18 months of age, with moderate-to-severe non-synostotic positional head shape deformities, including infants with plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads by applying mild pressure to prominent regions of the infant's cranium in order to improve cranial symmetry and/or shape. This device is also indicated for adjunctive use for infants from 3 to 18 months of age whose synostosis has been surgically corrected, but who still have moderate-to-severe cranial deformities including plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads. The STARband® Bi-Valve is made with an outer copolymer plastic shell and an inner liner made of pelite polyethylene foam or Aliplast foam (closed cell polyethylene). It utilizes an overlapping bi-valve design with a sliding mechanism and is held in place by a Velcro® strap.
ORTHOMERICA PRODUCTS, INC.
703.06PA
In Commercial Distribution
- B15170306PA0 ()
703.06PA
- Cranial orthosis
The STARband® Bi-Valve is a patient specific cranial orthosis that redirects the head growth to improve proportion and symmetry. It is intended for use on infants from 3 to 18 months of age, with moderate-to-severe non-synostotic positional head shape deformities, including infants with plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads by applying mild pressure to prominent regions of the infant's cranium in order to improve cranial symmetry and/or shape. This device is also indicated for adjunctive use for infants from 3 to 18 months of age whose synostosis has been surgically corrected, but who still have moderate-to-severe cranial deformities including plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads. The STARband® Bi-Valve is made with an outer copolymer plastic shell and an inner liner made of pelite polyethylene foam or Aliplast foam (closed cell polyethylene). It utilizes an overlapping bi-valve design with a sliding mechanism and is held in place by a Velcro® strap.
ORTHOMERICA PRODUCTS, INC.
703.06A
In Commercial Distribution
- B15170306A0 ()
703.06A
- Cranial orthosis
The Clarren Helmet is a patient specific cranial orthosis that applies passive pressure to prominent regions of an infant’s cranium in order to improve cranial symmetry and/or shape in infants from 3 to 18 months of age with moderate to severe nonsynostotic positional plagiocephaly, including infants with plagiocephalic, brachycephalic, and scaphocephalic- shaped heads. The Clarren Helmet is made with an outer polypropylene plastic shell with a Plastizote inner liner and a chinstrap to help hold the helmet in place.
ORTHOMERICA PRODUCTS, INC.
703.05A
In Commercial Distribution
- B15170305A0 ()
703.05A
- Cranial orthosis
The STARlight® is a patient specific cranial orthosis that redirects the head growth to improve proportion and symmetry. It is intended for use on infants from 3 to 18 months of age, with moderate-to-severe non-synostotic positional head shape deformities, including infants with plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads by applying mild pressure to prominent regions of the infant's cranium in order to improve cranial symmetry and/or shape. This device is also indicated for adjunctive use for infants from 3 to 18 months of age whose synostosis has been surgically corrected, but who still have moderate-to-severe cranial deformities including plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads. The STARlight® is made of clear Surlyn plastic or clear co-polyester plastic and may contain optional Aliplast foam (closed cell polyethylene) padding. It utilizes a side opening design and is held in place by a Velcro® strap across the side opening.
ORTHOMERICA PRODUCTS, INC.
703.03A
In Commercial Distribution
- B15170303A0 ()
703.03A
- Cranial orthosis
The STARlight® Bi-Valve is a patient specific cranial orthosis that redirects the head growth to improve proportion and symmetry. It is intended for use on infants from 3 to 18 months of age, with moderate-to-severe non-synostotic positional head shape deformities, including infants with plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads by applying mild pressure to prominent regions of the infant's cranium in order to improve cranial symmetry and/or shape. This device is also indicated for adjunctive use for infants from 3 to 18 months of age whose synostosis has been surgically corrected, but who still have moderate-to-severe cranial deformities including plagiocephalic-, brachycephalic- and scaphocephalic-shaped heads. The STARlight® Bi-Valve is made of clear Surlyn plastic or clear co-polyester plastic and may contain optional Aliplast foam (closed cell polyethylene) padding. It utilizes an overlapping bi-valve design with a sliding mechanism and is held in place by a Velcro® strap.
ORTHOMERICA PRODUCTS, INC.
703.01PA
In Commercial Distribution
- B15170301PA0 ()
703.01PA
- Cranial orthosis
The Non-cannulated Glenoid Reamer is used to compress and/or remove bone to create a cavity of proper shape and size for the implant.
Ascension Orthopedics, Inc.
RMR-0926-03N
In Commercial Distribution
- M269RMR092603N1 ()
- 10381780258728 ()
- Large
- Bone-resection orthopaedic reamer, reusable
The Non-cannulated Bowtie Reamer is used to compress and/or remove bone to create a cavity of proper shape and size for the implant.
Ascension Orthopedics, Inc.
RMR-0926-03BN
In Commercial Distribution
- M269RMR092603BN1 ()
- 10381780258711 ()
- Large
- Bone-resection orthopaedic reamer, reusable
The Cannulated Glenoid Reamer is used to compress and/or remove bone to create a cavity of proper shape and size for the implant.
Ascension Orthopedics, Inc.
RMR-0926-03C
In Commercial Distribution
- M269RMR092603C1 ()
- 10381780258490 ()
- Large
- Bone-resection orthopaedic reamer, reusable
The Cannulated Bowtie Reamer is used to compress and/or remove bone to create a cavity of proper shape and size for the implant.
Ascension Orthopedics, Inc.
RMR-0926-03BC
In Commercial Distribution
- M269RMR092603BC1 ()
- 10381780258483 ()
- Large
- Bone-resection orthopaedic reamer, reusable
The Non-cannulated Glenoid Reamer is used to compress and/or remove bone to create a cavity of proper shape and size for the implant.
Ascension Orthopedics, Inc.
RMR-0926-02N
In Commercial Distribution
- M269RMR092602N1 ()
- 10381780258476 ()
- Medium
- Bone-resection orthopaedic reamer, reusable
The Cannulated Glenoid Reamer is used to compress and/or remove bone to create a cavity of proper shape and size for the implant.
Ascension Orthopedics, Inc.
RMR-0926-02C
In Commercial Distribution
- M269RMR092602C1 ()
- 10381780258469 ()
- Medium
- Bone-resection orthopaedic reamer, reusable
The Non-cannulated Bowtie Reamer is used to compress and/or remove bone to create a cavity of proper shape and size for the implant.
Ascension Orthopedics, Inc.
RMR-0926-02BN
In Commercial Distribution
- M269RMR092602BN1 ()
- 10381780258452 ()
- Medium
- Bone-resection orthopaedic reamer, reusable
The Cannulated Bowtie Reamer is used to compress and/or remove bone to create a cavity of proper shape and size for the implant.
Ascension Orthopedics, Inc.
RMR-0926-02BC
In Commercial Distribution
- M269RMR092602BC1 ()
- 10381780258445 ()
- Medium
- Bone-resection orthopaedic reamer, reusable
The Non-cannulated Glenoid Reamer is used to compress and/or remove bone to create a cavity of proper shape and size for the implant.
Ascension Orthopedics, Inc.
RMR-0926-01N
In Commercial Distribution
- M269RMR092601N1 ()
- 10381780258438 ()
- Small
- Bone-resection orthopaedic reamer, reusable
The Cannulated Glenoid Reamer is used to compress and/or remove bone to create a cavity of proper shape and size for the implant.
Ascension Orthopedics, Inc.
RMR-0926-01C
In Commercial Distribution
- M269RMR092601C1 ()
- 10381780258421 ()
- Small
- Bone-resection orthopaedic reamer, reusable
The Non-cannulated Bowtie Reamer is used to compress and/or remove bone to create a cavity of proper shape and size for the implant.
Ascension Orthopedics, Inc.
RMR-0926-01BN
In Commercial Distribution
- M269RMR092601BN1 ()
- 10381780258414 ()
- Small
- Bone-resection orthopaedic reamer, reusable
The Cannulated Bowtie Reamer is used to compress and/or remove bone to create a cavity of proper shape and size for the implant.
Ascension Orthopedics, Inc.
RMR-0926-01BC
In Commercial Distribution
- M269RMR092601BC1 ()
- 10381780258407 ()
- Small
- Bone-resection orthopaedic reamer, reusable
The Non-cannulated Glenoid Reamer is used to compress and/or remove bone to create a cavity of proper shape and size for the implant.
Ascension Orthopedics, Inc.
RMR-0926-00N
In Commercial Distribution
- M269RMR092600N1 ()
- 10381780258391 ()
- X-Small
- Bone-resection orthopaedic reamer, reusable
The Cannulated Glenoid Reamer is used to compress and/or remove bone to create a cavity of proper shape and size for the implant.
Ascension Orthopedics, Inc.
RMR-0926-00C
In Commercial Distribution
- M269RMR092600C1 ()
- 10381780258384 ()
- X-Small
- Bone-resection orthopaedic reamer, reusable
The Non-cannulated Bowtie Reamer is used to compress and/or remove bone to create a cavity of proper shape and size for the implant.
Ascension Orthopedics, Inc.
RMR-0926-00BN
In Commercial Distribution
- M269RMR092600BN1 ()
- 10381780258377 ()
- X-Small
- Bone-resection orthopaedic reamer, reusable
The Cannulated Bowtie Reamer is used to compress and/or remove bone to create a cavity of proper shape and size for the implant.
Ascension Orthopedics, Inc.
RMR-0926-00BC
In Commercial Distribution
- M269RMR092600BC1 ()
- 10381780258360 ()
- X-Small
- Bone-resection orthopaedic reamer, reusable
MAXCUT DIAMOND BURS (6/pk) Shape: Round End Cylinder; Size (in 1/10mm): 014; Grit: Fine; For more information: https://www.scottsdental.com/burs/diamond-burs/round-end-cylinder-multi-use-diamond-burs-maxcut.html
SCOTT'S DENTAL SUPPLY L.L.C.
100-8881-14
In Commercial Distribution
- D7781008881140 ()
- D7781008881141 ()
100-8881-14
- Diamond dental bur, reusable
MAXCUT DIAMOND BURS (6/pk) Shape: Round End Cylinder; Size (in 1/10mm): 012; Grit: Fine; For more information: https://www.scottsdental.com/burs/diamond-burs/round-end-cylinder-multi-use-diamond-burs-maxcut.html
SCOTT'S DENTAL SUPPLY L.L.C.
100-8881-12
In Commercial Distribution
- D7781008881120 ()
- D7781008881121 ()
100-8881-12
- Diamond dental bur, reusable
MAXCUT DIAMOND BURS (6/pk) Shape: Round End Taper; Size (in 1/10mm): 016; Grit: Fine; For more information: https://www.scottsdental.com/burs/diamond-burs/round-end-taper-multi-use-diamond-burs-maxcut.html
SCOTT'S DENTAL SUPPLY L.L.C.
100-8850-16
In Commercial Distribution
- D7781008850160 ()
- D7781008850161 ()
100-8850-16
- Diamond dental bur, reusable
MAXCUT DIAMOND BURS (6/pk) Shape: Round End Taper; Size (in 1/10mm): 012; Grit: Fine; For more information: https://www.scottsdental.com/burs/diamond-burs/round-end-taper-multi-use-diamond-burs-maxcut.html
SCOTT'S DENTAL SUPPLY L.L.C.
100-8850-12
In Commercial Distribution
- D7781008850120 ()
- D7781008850121 ()
100-8850-12
- Diamond dental bur, reusable