SEARCH RESULTS FOR: 制作AT(4100 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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AXSOS - 07613154485710

Plate Rack with Lid - Generic
Stryker GmbH
902829
In Commercial Distribution

  • 07613154485710 ()
902829

  • Surgical instrument/implant rack

AXSOS - 07613154485697

Plate Rack with Lid - Special Plates
Stryker GmbH
902828
In Commercial Distribution

  • 07613154485697 ()
902828

  • Surgical instrument/implant rack

AXSOS - 07613154485673

Plate Rack with Lid - Compression Plates
Stryker GmbH
902827
In Commercial Distribution

  • 07613154485673 ()
902827

  • Surgical instrument/implant rack

AXSOS - 07613154485598

Screw Rack with Lid - Locking
Stryker GmbH
902813
In Commercial Distribution

  • 07613154485598 ()
902813

  • Surgical instrument/implant rack

AXSOS - 07613154485550

Plate Rack with Lid - Special Plates
Stryker GmbH
902810
In Commercial Distribution

  • 07613154485550 ()
902810

  • Surgical instrument/implant rack

AXSOS - 07613154485536

Plate Rack with Lid - Compression Plates
Stryker GmbH
902809
In Commercial Distribution

  • 07613154485536 ()
902809

  • Surgical instrument/implant rack

OMEGA - 07613154482498

Basic Cortical Screw Rack
Stryker GmbH
902116
In Commercial Distribution

  • 07613154482498 ()
902116

  • Surgical instrument/implant rack

OMEGA - 07613154482481

Basic Locking Screw Rack
Stryker GmbH
902115
In Commercial Distribution

  • 07613154482481 ()
902115

  • Surgical instrument/implant rack

OMEGA - 07613154482412

Screw Rack with Lid
Stryker GmbH
902037
In Commercial Distribution

  • 07613154482412 ()
902037

  • Surgical instrument/implant rack

EARP INSTRUMENTS - 00810135961103

EARP RETRACTOR TRAY. 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-TRAY02-XXX
In Commercial Distribution

  • 00810135961103 ()


  • Surgical instrument/implant rack
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