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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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DBM in a Lipid Carrier with Porous Calcium Granules
Biomet Orthopedics, LLC
92-2006
In Commercial Distribution

  • 00880304683907 ()

  • Qty: 5 cc (Volume)
92-2006

  • Bone matrix implant, human-derived
Endometrial Suction Curette with Syringe
UTAH MEDICAL PRODUCTS, INC.
Clear
In Commercial Distribution

  • H671CUR1201 ()
  • H671CUR1200 ()

  • Syringe Volume - 20 cc
  • Length: 27 Centimeter
  • Outer Diameter: 3.1 Millimeter
CUR-120

  • Endometrial biopsy curette
Porous Hydroxyapatite Bone Graft Substitute
Biomet Orthopedics, LLC
DBM050
In Commercial Distribution

  • 00888480585206 ()

  • STERILE Granules, 15 cc
DBM050

  • Bone matrix implant, human-derived
Porous Hydroxyapatite Bone Graft Substitute
Biomet Orthopedics, LLC
2G15
In Commercial Distribution

  • 00888480584261 ()

  • STERILE Granules, 5 cc
2G15

  • Synthetic bone graft
No Description
WRIGHT MEDICAL TECHNOLOGY, INC.
86CP1200
In Commercial Distribution

  • 00840420134943 ()

  • Total Volume: 12 cc
  • Total Volume: 12 Milliliter
86CP1200

  • Bone matrix implant, human-derived
No Description
WRIGHT MEDICAL TECHNOLOGY, INC.
89000020
In Commercial Distribution

  • 00840420134257 ()

  • Total Volume: 20 cc
89000020

  • Bone matrix implant, synthetic, non-antimicrobial
No Description
WRIGHT MEDICAL TECHNOLOGY, INC.
89000015
In Commercial Distribution

  • 00840420133748 ()

  • Total Volume: 15 cc
89000015

  • Bone matrix implant, synthetic, non-antimicrobial
Synthetic Mineral Bone Graft for Dental Surgery 2.0cc / 1.0g
COLLAGEN MATRIX, INC.
SM10010
In Commercial Distribution

  • 00813954021751 ()

  • 2.0 cc / 1.0 g
SM10010

  • Synthetic bone graft
Device Name: CERASORB® M DENTAL lndications for Use: CERASORB® M DENTAL is recommended for: - Augmentation or reconstructive treatment of the alveolar ridge - Filling of infrabony periodontal defects - Filling of defects after root resection, apicoectomy and cystectomy - Filling of extraction sockets to enhance preservation of the alveolar ridge - Elevation of the maxillary sinus floor - Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR) - Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration (GBR)
curasan AG
1000-2000µm
In Commercial Distribution

  • ECURS20M1000 ()
  • ECURS20M10005 ()

  • Total Volume: 2.0 Centiliter
5 x 2.0 cc

  • Dental bone matrix implant, synthetic
Device Name: CERASORB® M DENTAL lndications for Use: CERASORB® M DENTAL is recommended for: - Augmentation or reconstructive treatment of the alveolar ridge - Filling of infrabony periodontal defects - Filling of defects after root resection, apicoectomy and cystectomy - Filling of extraction sockets to enhance preservation of the alveolar ridge - Elevation of the maxillary sinus floor - Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR) - Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration (GBR)
curasan AG
500-1000µm
In Commercial Distribution

  • ECURS20M0500 ()
  • ECUS20M05005 ()

  • Total Volume: 2.0 Centiliter
5 x 2.0 cc

  • Dental bone matrix implant, synthetic
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