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Sterile disposable microkeratome blade, for use on the Moria® C-B Microkeratome, Sample
MED LOGICS INC
ML7020 (-20)
In Commercial Distribution
- 00850724001216 ()
- 10850724001213 ()
ML7020 (-20)
- Keratome blade, single-use
Sterile disposable microkeratome blade, for use on the Amadeus® Microkeratome, Sample
MED LOGICS INC
ML7090 (+20)
In Commercial Distribution
- 00850724001186 ()
- 10850724001183 ()
ML7090 (+20)
- Keratome blade, single-use
Sterile disposable microkeratome blade, for use on the MED-LOGICS ML7™ Microkeratome, Sample
MED LOGICS INC
ML7100 (-20)
In Commercial Distribution
- 00850724001056 ()
- 10850724001053 ()
ML7100 (-20)
- Keratome blade, single-use
This is a medical device.The dental treatment unit running as a desktop unit is intended for use in the field of dentistry. It is designed for the operation of an electrically operated small voltage motor. Area of application is in the field of endodontics and tooth preparation.
The ELECTROmatic is intended to convert pneumatic output from a dental treatment center to electrical energy for operation of electrically-driven dental handpieces. This device is designed for use by a trained professional in the field of general
dentistry.The ELECTROmatic dental control unit is a stand-alone system for operating electrically-driven KaVo handpieces. External power supply provides electric power to the unit. The 4-hole tubing connected to the unit supplies chip /cooling air, water and
pressure signal. The speed of the electric handpiece is controlled by air pressure. The control unit is positioned close to a treatment unit at thelocation preferred by the dentist. The ELECTROmatic system consists of a base unit with a motor hose, an
electrical motor, a transformer, and a power cord.
The dental treatment unit running as a desktop unit is intended for use in the field of dentistry. It is designed for the operation of an electrically operated small voltage motor. Area of application is in the field of endodontics and tooth preparation.
The ELECTROmatic is intended to convert pneumatic output from a dental treatment center to electrical energy for operation of electrically-driven dental handpieces. This device is designed for use by a trained professional in the field of general
dentistry.
KaVo Dental GmbH
1.003.1107
In Commercial Distribution
- EKAV100311070 ()
20 E
- Dental power tool system handpiece, line-powered
No Description
BIOCARE MEDICAL LLC
CM062C
In Commercial Distribution
- 00847627005830 ()
- Cytokeratin IVD, antibody
No Description
BIOCARE MEDICAL LLC
CM062A
In Commercial Distribution
- 00847627005823 ()
- Cytokeratin IVD, antibody
No Description
BIOCARE MEDICAL LLC
IP062G10
In Commercial Distribution
- 00847627008541 ()
- Cytokeratin IVD, antibody
No Description
Dynarex Corporation
4140
In Commercial Distribution
- 00616784414010 ()
- 00616784414027 ()
- 00616784414034 ()
- Manual scalpel blade, single-use
No Description
BIOCARE MEDICAL LLC
NPAI062T80
In Commercial Distribution
- 00847627039002 ()
- Cytokeratin IVD, antibody
No Description
BIOCARE MEDICAL LLC
NPAI062T40
In Commercial Distribution
- 00847627038999 ()
- Cytokeratin IVD, antibody
No Description
BIOCARE MEDICAL LLC
OPAI062T60
In Commercial Distribution
- 00847627024428 ()
- Cytokeratin IVD, antibody
The Vibrant Capsule is a small dimension, easy to swallow capsule, bearing pre-programed stimulations specifically designed for individuals with chronic constipation. Each box contains 2 blisters with capsules. Each blister contains 10 capsules.
VIBRANT LTD
1
In Commercial Distribution
- 00860009189805 ()
- Internal gastrointestinal vibratory-stimulation system capsule
20 Minute Biological Indicator, 25 Count
HU-FRIEDY MFG. CO., LLC
RR20BI
In Commercial Distribution
- 10889950139889 ()
- Biological sterilization indicator
20 Minute Reader Incubator
HU-FRIEDY MFG. CO., LLC
RR20READER
In Commercial Distribution
- 10889950139872 ()
- Test tube heater
20 GA/5000 CPM; Vitrectomy Pak
Alcon Laboratories, Inc.
8065751020
In Commercial Distribution
- 10380657510204 ()
- 00380657510207 ()
- 20 Gauge
- Vitrectomy system handpiece
No Description
BIOANALYTIC GmbH, biomed. Analysentechnik
003605-6005
In Commercial Distribution
- 04061609000033 ()
- 04061609000552 ()
- Sperm concentration indicator IVD, reagent
For microscopic counting of Sperms. (5 Tests)
BIOANALYTIC GmbH, biomed. Analysentechnik
003604-6005
In Commercial Distribution
- 04061609000019 ()
- 04061609000545 ()
- Sperm concentration indicator IVD, reagent
Leica Biosystems Accessory
Leica Biosystems Nussloch GmbH
000000014047534516
In Commercial Distribution
- 04049188060204 ()
- Device Size Text, specify:
14047534516
- Microscope slide stainer IVD
IMPLANT 20:1
SIRONA Dental Systems GmbH
6043702
Not in Commercial Distribution
- E27660437020 ()
- Dental surgical power tool motorized handpiece/set, pneumatic
No Description
SEBIA
4786
In Commercial Distribution
- 03607360047866 ()
4786
- Protein electrophoresis IVD, control
No Description
SEBIA
4766
In Commercial Distribution
- 03607360047668 ()
4766
- Protein electrophoresis IVD, control
No Description
G21 SRL
900199
In Commercial Distribution
- 08058964727596 ()
- Balloon kyphoplasty kit
No Description
T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION
B
In Commercial Distribution
- 10810190017927 ()
748221t
- Cast cutting shears
No Description
T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION
B
In Commercial Distribution
- 10810190017910 ()
748211
- Cast cutting shears
No Description
T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION
B
In Commercial Distribution
- 10810190017132 ()
391421t
- Clamp manipulation forceps
No Description
T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION
B
In Commercial Distribution
- 10810190017125 ()
391411t
- Clamp manipulation forceps
Synthetic Bone Substitute
Granules
BIOMATLANTE
RT0701M+GS50
In Commercial Distribution
- 03700501812870 ()
- Total Volume: 0.5 Milliliter
RT0701M+GS50
- Bone matrix implant, synthetic, non-antimicrobial
TORQUE MASTER 20 4-HOLE IS AN ADJUSTABLE SPEED UP TO 20000 RPM LOW SPEED PNEUMATIC DENTAL MOTOR, USED IN CONJUNCTION WITH OTHER ATTACHMENTS SUCH AS BURS AND MANDRELS WHICH CONNECTS TO AN OPERATORY TO DRILL BONE, TEETH AND TOUGH TISSUES IN A DENTAL SETTING. REMOVING CALCULUS AND POLISHING TEEETH
MTI Precision Products, LLC
TM204
In Commercial Distribution
- D826TM2040 ()
- D826TM204 ()
- Dental surgical power tool motor, pneumatic
TORQUE MASTER 20 2-HOLE IS AN ADJUSTABLE SPEED UP TO 20000 RPM LOW SPEED PNEUMATIC DENTAL MOTOR, USED IN CONJUNCTION WITH OTHER ATTACHMENTS SUCH AS BURS AND MANDRELS WHICH CONNECTS TO AN OPERATORY TO DRILL BONE, TEETH AND TOUGH TISSUES IN A DENTAL SETTING. REMOVING CALCULUS AND POLISHING TEEETH
MTI Precision Products, LLC
TM202
In Commercial Distribution
- D826TM2020 ()
- D826TM202 ()
- Dental surgical power tool motor, pneumatic
No Description
SAMSUNG MEDISON CO., LTD.
USP-CZ24EAA/WR
In Commercial Distribution
- 08806167740122 ()
- Extracorporeal ultrasound imaging transducer, hand-held
SUPERSONIC MACH 20
Supersonic Imagine, Inc.
SSIP95020-HOLX
In Commercial Distribution
- 03760193600230 ()
SSIP95020-HOLX
- General-purpose ultrasound imaging system
The SIGNUS TETRIS™ ST and SIGNUS TETRIS™ R ST system is an intervertebral fusion device to treat degenerative disc disease. The implants are additively manufactured from titanium alloy (Ti-6Al-4V). Each device is available in a single footprint, with multiple heights and angulations. The SIGNUS TETRIS™ ST/ TETRIS™ R ST device is placed by a PLIF (Posterior Lumbar Interbody Fusion) approach in the L2 – S1 spinal region and should be inserted in pairs. The device is comprised of structural titanium in an open-pore grid structure. The large fenestration in the implant permits the cage to be packed with autogenous bone graft and/or allograft comprised of cancellous and/or corticocancellous bone graft to facilitate fusion.
SIGNUS Medizintechnik GmbH
Lumbar cage, angled
In Commercial Distribution
- 04047844114254 ()
- 17x10x32mm
TST20171032
- Metallic spinal interbody fusion cage
The SIGNUS TETRIS™ ST and SIGNUS TETRIS™ R ST system is an intervertebral fusion device to treat degenerative disc disease. The implants are additively manufactured from titanium alloy (Ti-6Al-4V). Each device is available in a single footprint, with multiple heights and angulations. The SIGNUS TETRIS™ ST/ TETRIS™ R ST device is placed by a PLIF (Posterior Lumbar Interbody Fusion) approach in the L2 – S1 spinal region and should be inserted in pairs. The device is comprised of structural titanium in an open-pore grid structure. The large fenestration in the implant permits the cage to be packed with autogenous bone graft and/or allograft comprised of cancellous and/or corticocancellous bone graft to facilitate fusion.
SIGNUS Medizintechnik GmbH
Lumbar cage, angled
In Commercial Distribution
- 04047844114247 ()
- 16x10x32mm
TST20161032
- Metallic spinal interbody fusion cage
The SIGNUS TETRIS™ ST and SIGNUS TETRIS™ R ST system is an intervertebral fusion device to treat degenerative disc disease. The implants are additively manufactured from titanium alloy (Ti-6Al-4V). Each device is available in a single footprint, with multiple heights and angulations. The SIGNUS TETRIS™ ST/ TETRIS™ R ST device is placed by a PLIF (Posterior Lumbar Interbody Fusion) approach in the L2 – S1 spinal region and should be inserted in pairs. The device is comprised of structural titanium in an open-pore grid structure. The large fenestration in the implant permits the cage to be packed with autogenous bone graft and/or allograft comprised of cancellous and/or corticocancellous bone graft to facilitate fusion.
SIGNUS Medizintechnik GmbH
Lumbar cage, angled
In Commercial Distribution
- 04047844114230 ()
- 15x10x32mm
TST20151032
- Metallic spinal interbody fusion cage
The SIGNUS TETRIS™ ST and SIGNUS TETRIS™ R ST system is an intervertebral fusion device to treat degenerative disc disease. The implants are additively manufactured from titanium alloy (Ti-6Al-4V). Each device is available in a single footprint, with multiple heights and angulations. The SIGNUS TETRIS™ ST/ TETRIS™ R ST device is placed by a PLIF (Posterior Lumbar Interbody Fusion) approach in the L2 – S1 spinal region and should be inserted in pairs. The device is comprised of structural titanium in an open-pore grid structure. The large fenestration in the implant permits the cage to be packed with autogenous bone graft and/or allograft comprised of cancellous and/or corticocancellous bone graft to facilitate fusion.
SIGNUS Medizintechnik GmbH
Lumbar cage, angled
In Commercial Distribution
- 04047844114162 ()
- 18x10x32mm
TST20181032
- Metallic spinal interbody fusion cage
The SIGNUS TETRIS™ ST and SIGNUS TETRIS™ R ST system is an intervertebral fusion device to treat degenerative disc disease. The implants are additively manufactured from titanium alloy (Ti-6Al-4V). Each device is available in a single footprint, with multiple heights and angulations. The SIGNUS TETRIS™ ST/ TETRIS™ R ST device is placed by a PLIF (Posterior Lumbar Interbody Fusion) approach in the L2 – S1 spinal region and should be inserted in pairs. The device is comprised of structural titanium in an open-pore grid structure. The large fenestration in the implant permits the cage to be packed with autogenous bone graft and/or allograft comprised of cancellous and/or corticocancellous bone graft to facilitate fusion.
SIGNUS Medizintechnik GmbH
Lumbar cage, angled
In Commercial Distribution
- 04047844113769 ()
- 17x10x28mm
TST20171028
- Metallic spinal interbody fusion cage
The SIGNUS TETRIS™ ST and SIGNUS TETRIS™ R ST system is an intervertebral fusion device to treat degenerative disc disease. The implants are additively manufactured from titanium alloy (Ti-6Al-4V). Each device is available in a single footprint, with multiple heights and angulations. The SIGNUS TETRIS™ ST/ TETRIS™ R ST device is placed by a PLIF (Posterior Lumbar Interbody Fusion) approach in the L2 – S1 spinal region and should be inserted in pairs. The device is comprised of structural titanium in an open-pore grid structure. The large fenestration in the implant permits the cage to be packed with autogenous bone graft and/or allograft comprised of cancellous and/or corticocancellous bone graft to facilitate fusion.
SIGNUS Medizintechnik GmbH
Lumbar cage, angled
In Commercial Distribution
- 04047844113752 ()
- 18x10x28mm
TST20181028
- Metallic spinal interbody fusion cage
The SIGNUS TETRIS™ ST and SIGNUS TETRIS™ R ST system is an intervertebral fusion device to treat degenerative disc disease. The implants are additively manufactured from titanium alloy (Ti-6Al-4V). Each device is available in a single footprint, with multiple heights and angulations. The SIGNUS TETRIS™ ST/ TETRIS™ R ST device is placed by a PLIF (Posterior Lumbar Interbody Fusion) approach in the L2 – S1 spinal region and should be inserted in pairs. The device is comprised of structural titanium in an open-pore grid structure. The large fenestration in the implant permits the cage to be packed with autogenous bone graft and/or allograft comprised of cancellous and/or corticocancellous bone graft to facilitate fusion.
SIGNUS Medizintechnik GmbH
Lumbar cage, angled
In Commercial Distribution
- 04047844113745 ()
- 15x10x28mm
TST20151028
- Metallic spinal interbody fusion cage
The SIGNUS TETRIS™ ST and SIGNUS TETRIS™ R ST system is an intervertebral fusion device to treat degenerative disc disease. The implants are additively manufactured from titanium alloy (Ti-6Al-4V). Each device is available in a single footprint, with multiple heights and angulations. The SIGNUS TETRIS™ ST/ TETRIS™ R ST device is placed by a PLIF (Posterior Lumbar Interbody Fusion) approach in the L2 – S1 spinal region and should be inserted in pairs. The device is comprised of structural titanium in an open-pore grid structure. The large fenestration in the implant permits the cage to be packed with autogenous bone graft and/or allograft comprised of cancellous and/or corticocancellous bone graft to facilitate fusion.
SIGNUS Medizintechnik GmbH
Lumbar cage, angled
In Commercial Distribution
- 04047844113738 ()
- 14x10x28mm
TST20141028
- Metallic spinal interbody fusion cage
The SIGNUS TETRIS™ ST and SIGNUS TETRIS™ R ST system is an intervertebral fusion device to treat degenerative disc disease. The implants are additively manufactured from titanium alloy (Ti-6Al-4V). Each device is available in a single footprint, with multiple heights and angulations. The SIGNUS TETRIS™ ST/ TETRIS™ R ST device is placed by a PLIF (Posterior Lumbar Interbody Fusion) approach in the L2 – S1 spinal region and should be inserted in pairs. The device is comprised of structural titanium in an open-pore grid structure. The large fenestration in the implant permits the cage to be packed with autogenous bone graft and/or allograft comprised of cancellous and/or corticocancellous bone graft to facilitate fusion.
SIGNUS Medizintechnik GmbH
Lumbar cage, angled
In Commercial Distribution
- 04047844113721 ()
- 16x10x28mm
TST20161028
- Metallic spinal interbody fusion cage