SEARCH RESULTS FOR: (*Forged New Hampshire driver*)(705478 results)

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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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OPTEFORM® Allograft Paste, 5cc - 10885862094230

No Description
Rti Surgical, Inc.
005105
In Commercial Distribution

  • 10885862094230 ()
606-01-05

  • Bone matrix implant, human-derived

OPTEFORM® Allograft Paste, 2cc - 10885862094223

No Description
Rti Surgical, Inc.
005102
In Commercial Distribution

  • 10885862094223 ()
606-01-02

  • Bone matrix implant, human-derived

OPTEFORM® Allograft Partial Disc, 90mm x 5mm, 22cc - 10885862094100

No Description
Rti Surgical, Inc.
002590
In Commercial Distribution

  • 10885862094100 ()
602-05-90

  • Bone matrix implant, human-derived

OPTEFORM® Allograft Partial Disc, 75mm x 5mm, 15cc - 10885862094094

No Description
Rti Surgical, Inc.
002575
In Commercial Distribution

  • 10885862094094 ()
602-05-75

  • Bone matrix implant, human-derived

OPTEFORM® Allograft Full Disc, 5 x 90mm, 32cc - 10885862093226

No Description
Rti Surgical, Inc.
002529
In Commercial Distribution

  • 10885862093226 ()
600-05-90

  • Bone matrix implant, human-derived

OPTEFORM® Allograft Disc, 45mm x 5mm, 8cc - 10885862093219

No Description
Rti Surgical, Inc.
002545
In Commercial Distribution

  • 10885862093219 ()
600-05-45

  • Bone matrix implant, human-derived

OPTEFORM® Allograft Disc, 30mm x 3mm, 2cc - 10885862093202

No Description
Rti Surgical, Inc.
002530
In Commercial Distribution

  • 10885862093202 ()
600-03-30

  • Bone matrix implant, human-derived

OPTEFORM® Allograft Full Disc, 3 x 20mm, 1cc - 10885862093196

No Description
Rti Surgical, Inc.
002523
In Commercial Distribution

  • 10885862093196 ()
600-03-20

  • Bone matrix implant, human-derived

OPTEFIL® Allograft Paste, 10cc - 10885862094407

No Description
Rti Surgical, Inc.
005010
In Commercial Distribution

  • 10885862094407 ()
616-01-10

  • Bone matrix implant, human-derived

Tinnitus Masker - 00089518000801

The Tinnitus custom device utilizes advanced digital signal processing with broadband white or pink noise integrated into a cosmetically appealing design. Designed for patients that suffer from Tinnitus to ease ringing in the ear.
GENERAL HEARING INSTRUMENT, INC.
Tinnitus,Custom,Pair
In Commercial Distribution

  • 00089518000801 ()


  • Air-conduction tinnitus masker, in-the-ear
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