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EARP FINAL INSERTER. 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-FI
In Commercial Distribution
- 00810135960632 ()
- General internal orthopaedic fixation system implantation kit
EARP INITIAL INSERTER. 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-II
In Commercial Distribution
- 00810135960625 ()
- General internal orthopaedic fixation system implantation kit
EARP DISC SPACER INSERTER. 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-DS-002
In Commercial Distribution
- 00810135960618 ()
- General internal orthopaedic fixation system implantation kit
Syringe Rack: LARGE, Holds 16 20cc-60cc Volume Syringes
Medco Manufacturing LLC
SR60-L-16
In Commercial Distribution
- 00810130450176 ()
- Test tube rack
Slip Joint Pliers 8"
Modern Surgical Instruments LLC
48-0262
In Commercial Distribution
- 00810130206377 ()
- Surgical flat-nosed pliers
PLIERS, NEEDLE NOSE 5 1/2"
Modern Surgical Instruments LLC
48-0245
In Commercial Distribution
- 00810130206360 ()
- Wire holding/twisting pliers
MAYO HEGAR N.H. 7" SERR CARB.
Modern Surgical Instruments LLC
41-0308
In Commercial Distribution
- 00810130206346 ()
- Suturing needle holder, reusable
Cottonoid Plate
Modern Surgical Instruments LLC
FSP3379
In Commercial Distribution
- 00810130206216 ()
- Instrument tray, reusable
Stiletto Osteotome Rack 9 1/2", holds 5 8 1/2" Stiletto Osteotomes 1/4"-3/4" [6mm-19mm]
Modern Surgical Instruments LLC
98.6048
In Commercial Distribution
- 00810130206056 ()
- Sterilization stringer
LISTON AMPUTATING KNIFE 8"
Modern Surgical Instruments LLC
46-0600
In Commercial Distribution
- 00810130206001 ()
- Amputation knife