SEARCH RESULTS FOR: 仿制AT(4093 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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DS OmniTaper - 07392532255472

OmniTaper Washtray Overlay GS
Dentsply Implants Manufacturing GmbH
68015355
In Commercial Distribution

  • 07392532255472 ()
68015355

  • Surgical instrument/implant rack

DS OmniTaper - 07392532255465

OmniTaper Washtray GS
Dentsply Implants Manufacturing GmbH
68015354
In Commercial Distribution

  • 07392532255465 ()
68015354

  • Surgical instrument/implant rack

DS OmniTaper - 07392532255458

OmniTaper Washtray Overlay
Dentsply Implants Manufacturing GmbH
68015272
In Commercial Distribution

  • 07392532255458 ()
68015272

  • Surgical instrument/implant rack

DS OmniTaper - 07392532255441

OmniTaper Washtray
Dentsply Implants Manufacturing GmbH
68015271
In Commercial Distribution

  • 07392532255441 ()
68015271

  • Surgical instrument/implant rack

PrimeTaper - 07392532253010

PrimeTaper Surgical Tray
Dentsply Implants Manufacturing GmbH
68011090
In Commercial Distribution

  • 07392532253010 ()
68015322

  • Surgical instrument/implant rack

DS OmniTaper - 07392532253003

OmniTaper Surgical Tray GS
Dentsply Implants Manufacturing GmbH
68017203
In Commercial Distribution

  • 07392532253003 ()
68017203

  • Surgical instrument/implant rack

DS OmniTaper - 07392532252990

OmniTaper Surgical Tray
Dentsply Implants Manufacturing GmbH
68015282
In Commercial Distribution

  • 07392532252990 ()
68015282

  • Surgical instrument/implant rack

FRIADENT® - 07392532231889

Prosthetic Tray Mini empty
Dentsply Implants Manufacturing GmbH
46-7001
In Commercial Distribution

  • 07392532231889 ()
46-7001

  • Surgical instrument/implant rack

EARP INSTRUMENTS - 00810135960922

EARP, DISC SPACER CADDIE. The EARP Interbody System is intended for intervertebral body fusion in the lumbar spine in skeletally mature patients with degenerative disc disease (DDD) at one or two contiguous levels from L2 to S1 of the lumbosacral spine. DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment prior to treatment with an intervertebral cage. DDD patients may also have Grade 1 spondylolisthesis or retrolisthesis at involved levels. The device system must be used with supplemental fixation and autograft to facilitate fusion and is implanted via a posterolateral approach.
NVISION BIOMEDICAL TECHNOLOGIES, INC.
EARP-DC
In Commercial Distribution

  • 00810135960922 ()


  • Surgical instrument/implant rack

Patient-Fitted TMJ Reconstructive Prosthesis System - B0046005200

Sterilization Case Instrument Base
TMJ Solutions, Inc.
60-0520
In Commercial Distribution

  • B0046005200 ()


  • Surgical instrument/implant rack
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