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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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SFAM803 ePTFE Block 1.5cm X 7cm
SURGICAL TECHNOLOGY LABORATORIES INC
SFAM803
In Commercial Distribution

  • 00854804007013 ()
SFAM803

  • PTFE/carbon-fibre craniofacial tissue reconstructive material
SFAM603 ePTFE Block 1.5cm x 7cm
SURGICAL TECHNOLOGY LABORATORIES INC
SFAM603
In Commercial Distribution

  • 00854804007006 ()
SFAM603

  • PTFE/carbon-fibre craniofacial tissue reconstructive material
GOLD OVERCASTING CAP PCA Ø4.8 Giving the negative shape of the permanent abutment for the design and realization by casting (lost wax process) of a dental restoration.
ETABLISSEMENTS ANTHOGYR
OPAC400
In Commercial Distribution

  • 03663394000376 ()

  • Outer Diameter: 4.8 Millimeter


  • Dental implant suprastructure, permanent, preformed
GOLD OVERCASTING CAP PC Ø4.0 Giving the negative shape of the permanent abutment for the design and realization by casting (lost wax process) of a dental restoration.
ETABLISSEMENTS ANTHOGYR
OPSC400
In Commercial Distribution

  • 03663394001892 ()

  • Outer Diameter: 4.0 Millimeter


  • Dental implant suprastructure, permanent, preformed
Regenomer® is a sponge-like absorbable and porous collagen designed to be used as bone filling augmentation material. The device is manufactured from purified type I collagen derived from porcine skin sources in South Korea. The porcine skin is certified by veterinarian and is obtained by a standardized controlled manufacturing process. Regenomer® is manufactured in three types, Regenomer® Syringe (sheet shape in syringe and blister), Regenomer® Plug (bullet shape in blister), and Regenomer® Block (block shape in blister). Regenomer® are supplied sterile, non-pyrogenic, and for single use only.
Nibec Co., Ltd.
RSP2-L
In Commercial Distribution

  • 08809186549455 ()

  • 12mm X 25mm


  • Dental bone matrix implant, animal-derived
Regenomer® is a sponge-like absorbable and porous collagen designed to be used as bone filling augmentation material. The device is manufactured from purified type I collagen derived from porcine skin sources in South Korea. The porcine skin is certified by veterinarian and is obtained by a standardized controlled manufacturing process. Regenomer® is manufactured in three types, Regenomer® Syringe (sheet shape in syringe and blister), Regenomer® Plug (bullet shape in blister), and Regenomer® Block (block shape in blister). Regenomer® are supplied sterile, non-pyrogenic, and for single use only.
Nibec Co., Ltd.
RSP1-S
In Commercial Distribution

  • 08809186549448 ()

  • 8mm X 18mm


  • Dental bone matrix implant, animal-derived
Regenomer® is a sponge-like absorbable and porous collagen designed to be used as bone filling augmentation material. The device is manufactured from purified type I collagen derived from porcine skin sources in South Korea. The porcine skin is certified by veterinarian and is obtained by a standardized controlled manufacturing process. Regenomer® is manufactured in three types, Regenomer® Syringe (sheet shape in syringe and blister), Regenomer® Plug (bullet shape in blister), and Regenomer® Block (block shape in blister). Regenomer® are supplied sterile, non-pyrogenic, and for single use only.
Nibec Co., Ltd.
RSB2-L
In Commercial Distribution

  • 08809186549431 ()

  • 8mm X 7mm X 9mm


  • Dental bone matrix implant, animal-derived
Regenomer® is a sponge-like absorbable and porous collagen designed to be used as bone filling augmentation material. The device is manufactured from purified type I collagen derived from porcine skin sources in South Korea. The porcine skin is certified by veterinarian and is obtained by a standardized controlled manufacturing process. Regenomer® is manufactured in three types, Regenomer® Syringe (sheet shape in syringe and blister), Regenomer® Plug (bullet shape in blister), and Regenomer® Block (block shape in blister). Regenomer® are supplied sterile, non-pyrogenic, and for single use only.
Nibec Co., Ltd.
RSB1-S
In Commercial Distribution

  • 08809186549424 ()

  • 6mm X 5mm X 7mm


  • Dental bone matrix implant, animal-derived
Flexible Adjustable Annuloplasty Ring
ST. JUDE MEDICAL, INC.
AFR-43
In Commercial Distribution

  • 05414734052177 ()

  • Outer Diameter: 43 Millimeter
AFR-43

  • Mitral/tricuspid annuloplasty ring, open-surgery
Flexible Adjustable Annuloplasty Ring
ST. JUDE MEDICAL, INC.
AFR-41
In Commercial Distribution

  • 05414734052160 ()

  • Outer Diameter: 41 Millimeter
AFR-41

  • Mitral/tricuspid annuloplasty ring, open-surgery
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