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OPEN END U STRINGER 10"
INTERNATIONAL SURGICAL PRODUCTS INC
U-OE-ST10
In Commercial Distribution
- 00810129330236 ()
- Sterilization stringer
8" L x 2.75" W PIN & SOCKET INSTRUMENT STRINGER
INTERNATIONAL SURGICAL PRODUCTS INC
STPS25-8
In Commercial Distribution
- 00810129330229 ()
- Sterilization stringer
6" L x 2.75" W PIN & SOCKET INSTRUMENT STRINGER
INTERNATIONAL SURGICAL PRODUCTS INC
STPS25-6
In Commercial Distribution
- 00810129330212 ()
- Sterilization stringer
12" L x 2.75" W PIN & SOCKET INSTRUMENT STRINGER
INTERNATIONAL SURGICAL PRODUCTS INC
STPS25-12
In Commercial Distribution
- 00810129330205 ()
- Sterilization stringer
10" L x 2.75" W PIN & SOCKET INSTRUMENT STRINGER
INTERNATIONAL SURGICAL PRODUCTS INC
STPS25-10
In Commercial Distribution
- 00810129330199 ()
- Sterilization stringer
8" PIN & SOCKET STRINGER 2.75" C TO C 3" DISTAL WIDTH
INTERNATIONAL SURGICAL PRODUCTS INC
STPS-8
In Commercial Distribution
- 00810129330182 ()
- Sterilization stringer
6" PIN & SOCKET STRINGER 2.75" C TO C 3" DISTAL WIDTH
INTERNATIONAL SURGICAL PRODUCTS INC
STPS-6
In Commercial Distribution
- 00810129330175 ()
- Sterilization stringer
12" PIN & SOCKET STRINGER 2.75" C TO C 3" DISTAL WIDTH
INTERNATIONAL SURGICAL PRODUCTS INC
STPS-12
In Commercial Distribution
- 00810129330168 ()
- Sterilization stringer
10" PIN & SOCKET STRINGER 2.75" C TO C 3" DISTAL WIDTH
INTERNATIONAL SURGICAL PRODUCTS INC
STPS-10
In Commercial Distribution
- 00810129330151 ()
- Sterilization stringer
8" L x 5.75" W CENTER LATCH INSTRUMENT STRINGER
INTERNATIONAL SURGICAL PRODUCTS INC
STCL55-8
In Commercial Distribution
- 00810129330144 ()
- Sterilization stringer
6" L x 5.75" W CENTER LATCH INSTRUMENT STRINGER
INTERNATIONAL SURGICAL PRODUCTS INC
STCL55-6
In Commercial Distribution
- 00810129330137 ()
- Sterilization stringer
16" L x 5.75" W CENTER LATCH INSTRUMENT STRINGER
INTERNATIONAL SURGICAL PRODUCTS INC
STCL55-16
In Commercial Distribution
- 00810129330120 ()
- Sterilization stringer
14" L x 5.75" W CENTER LATCH INSTRUMENT STRINGER
INTERNATIONAL SURGICAL PRODUCTS INC
STCL55-14
In Commercial Distribution
- 00810129330113 ()
- Sterilization stringer
12" L x 5.75" W CENTER LATCH INSTRUMENT STRINGER
INTERNATIONAL SURGICAL PRODUCTS INC
STCL55-12
In Commercial Distribution
- 00810129330106 ()
- Sterilization stringer
10" L x 5.75" W CENTER LATCH INSTRUMENT STRINGER
INTERNATIONAL SURGICAL PRODUCTS INC
STCL55-10
In Commercial Distribution
- 00810129330090 ()
- Sterilization stringer
8" L x 3" W CENTER LATCH INSTRUMENT STRINGER
INTERNATIONAL SURGICAL PRODUCTS INC
STCL-8
In Commercial Distribution
- 00810129330083 ()
- Sterilization stringer
6" L x 3" W CENTER LATCH INSTRUMENT STRINGER
INTERNATIONAL SURGICAL PRODUCTS INC
STCL-6
In Commercial Distribution
- 00810129330076 ()
- Sterilization stringer
18" L x 3" W CENTER LATCH INSTRUMENT STRINGER
INTERNATIONAL SURGICAL PRODUCTS INC
STCL-18
In Commercial Distribution
- 00810129330069 ()
- Sterilization stringer
16" L x 3" W CENTER LATCH INSTRUMENT STRINGER
INTERNATIONAL SURGICAL PRODUCTS INC
STCL-16
In Commercial Distribution
- 00810129330052 ()
- Sterilization stringer
14" L x 3" W CENTER LATCH INSTRUMENT STRINGER
INTERNATIONAL SURGICAL PRODUCTS INC
STCL-14
In Commercial Distribution
- 00810129330045 ()
- Sterilization stringer
12" L x 3" W CENTER LATCH INSTRUMENT STRINGER
INTERNATIONAL SURGICAL PRODUCTS INC
STCL-12
In Commercial Distribution
- 00810129330038 ()
- Sterilization stringer
10" L x 3" W CENTER LATCH INSTRUMENT STRINGER
INTERNATIONAL SURGICAL PRODUCTS INC
STCL-10
In Commercial Distribution
- 00810129330021 ()
- Sterilization stringer
8" L x 2.75" W BALL & SOCKET INSTRUMENT STRINGER
INTERNATIONAL SURGICAL PRODUCTS INC
STBS-8
In Commercial Distribution
- 00810129330014 ()
- Sterilization stringer
6" L x 2.75" W BALL & SOCKET INSTRUMENT STRINGER
INTERNATIONAL SURGICAL PRODUCTS INC
STBS-6
In Commercial Distribution
- 00810129330007 ()
- Sterilization stringer
No Description
Biomet Orthopedics, LLC
32-486800
In Commercial Distribution
- 00887868495083 ()
32-486800
- Surgical instrument handle, non-torque-limiting
No Description
Biomet Orthopedics, LLC
32-485020
In Commercial Distribution
- 00887868493638 ()
32-485020
- Surgical instrument handle, non-torque-limiting
No Description
Biomet Orthopedics, LLC
32-484060
In Commercial Distribution
- 00887868491641 ()
32-484060
- Surgical instrument handle, non-torque-limiting
No Description
Biomet Orthopedics, LLC
32-481030
In Commercial Distribution
- 00887868489105 ()
32-481030
- Surgical instrument handle, non-torque-limiting
Polypropylene Auto Adjustable Flex Syringe Rack Link System
Medco Manufacturing LLC
SR1-60-FLEX
In Commercial Distribution
- 00810130454570 ()
- Test tube rack
Syringe Rack: MEDIUM, Holds 40 1cc-20cc Volume Syringes
Medco Manufacturing LLC
SR10-M-40
In Commercial Distribution
- 00810130453603 ()
- Test tube rack
EARP DISC RAKE ANGLED.
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-DRA
In Commercial Distribution
- 00810135961059 ()
- Width: 35 Millimeter
- Depth: 22 Millimeter
- Height: 14 Millimeter
- General internal orthopaedic fixation system implantation kit
EARP, TRIAL 22X35X10 6°
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-T-2235-0610
In Commercial Distribution
- 00810135960861 ()
- Width: 35 Millimeter
- Depth: 22 Millimeter
- Height: 10 Millimeter
- General internal orthopaedic fixation system implantation kit
EARP, TRIAL 18X35X14 12°
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-T-1835-1214
In Commercial Distribution
- 00810135960854 ()
- Width: 35 Millimeter
- Depth: 18 Millimeter
- Height: 14 Millimeter
- General internal orthopaedic fixation system implantation kit
EARP, TRIAL 18X35X12 12°
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-T-1835-1212
In Commercial Distribution
- 00810135960847 ()
- Width: 35 Millimeter
- Depth: 18 Millimeter
- Height: 12 Millimeter
- General internal orthopaedic fixation system implantation kit
EARP, TRIAL 18X35X14 6°
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-T-1835-0614
In Commercial Distribution
- 00810135960830 ()
- Width: 35 Millimeter
- Depth: 18 Millimeter
- Height: 14 Millimeter
- General internal orthopaedic fixation system implantation kit
EARP, TRIAL 18X35X12 6°
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-T-1835-0612
In Commercial Distribution
- 00810135960823 ()
- Width: 35 Millimeter
- Depth: 18 Millimeter
- Height: 12 Millimeter
- General internal orthopaedic fixation system implantation kit
EARP, TRIAL 18X35X10 6°
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-T-1835-0610
In Commercial Distribution
- 00810135960816 ()
- Width: 35 Millimeter
- Depth: 18 Millimeter
- Height: 10 Millimeter
- General internal orthopaedic fixation system implantation kit
EARP, TRIAL 18X35X08 0°
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-T-1835-0008
In Commercial Distribution
- 00810135960809 ()
- Width: 35 Millimeter
- Depth: 18 Millimeter
- Height: 8 Millimeter
- General internal orthopaedic fixation system implantation kit
EARP, TRIAL 14X35X10 0°
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-T-1435-0010
In Commercial Distribution
- 00810135960793 ()
- Depth: 14 Millimeter
- Width: 35 Millimeter
- Height: 10 Millimeter
- General internal orthopaedic fixation system implantation kit
EARP, TRIAL 14X35X08 0°
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-T-1435-0008
In Commercial Distribution
- 00810135960786 ()
- Height: 8 Millimeter
- Depth: 14 Millimeter
- Width: 35 Millimeter
- General internal orthopaedic fixation system implantation kit
EARP, TRIAL 14X25X08 0°
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-T-1425-0008
In Commercial Distribution
- 00810135960779 ()
- Height: 8 Millimeter
- Width: 25 Millimeter
- Depth: 14 Millimeter
- General internal orthopaedic fixation system implantation kit
EARP Retractor, EARP BLADE 150.
The EARP Retractor is used in conjunction with TeDan Phantom ML MIS Lumbar Surgical Access System ML-2000 to assist with focal retraction, to increase working corridor and improve line of sight to working area.
NVISION BIOMEDICAL TECHNOLOGIES, INC.
EARP-R_001-150
In Commercial Distribution
- 00810135960748 ()
- Self-retaining surgical retractor, reusable
EARP Retractor, EARP BLADE 140.
The EARP Retractor is used in conjunction with TeDan Phantom ML MIS Lumbar Surgical Access System ML-2000 to assist with focal retraction, to increase working corridor and improve line of sight to working area.
NVISION BIOMEDICAL TECHNOLOGIES, INC.
EARP-R_001-140
In Commercial Distribution
- 00810135960731 ()
- Self-retaining surgical retractor, reusable
EARP Retractor, EARP BLADE 130.
The EARP Retractor is used in conjunction with TeDan Phantom ML MIS Lumbar Surgical Access System ML-2000 to assist with focal retraction, to increase working corridor and improve line of sight to working area.
NVISION BIOMEDICAL TECHNOLOGIES, INC.
EARP-R_001-130
In Commercial Distribution
- 00810135960724 ()
- Self-retaining surgical retractor, reusable
EARP Retractor, EARP BLADE 120.
The EARP Retractor is used in conjunction with TeDan Phantom ML MIS Lumbar Surgical Access System ML-2000 to assist with focal retraction, to increase working corridor and improve line of sight to working area.
NVISION BIOMEDICAL TECHNOLOGIES, INC.
EARP-R_001-120
In Commercial Distribution
- 00810135960717 ()
- Self-retaining surgical retractor, reusable
EARP Retractor, EARP BLADE 110.
The EARP Retractor is used in conjunction with TeDan Phantom ML MIS Lumbar Surgical Access System ML-2000 to assist with focal retraction, to increase working corridor and improve line of sight to working area.
NVISION BIOMEDICAL TECHNOLOGIES, INC.
EARP-R_001-110
In Commercial Distribution
- 00810135960700 ()
- Self-retaining surgical retractor, reusable
EARP Retractor, EARP BLADE 100
The EARP Retractor is used in conjunction with TeDan Phantom ML MIS Lumbar Surgical Access System ML-2000 to assist with focal retraction, to increase working corridor and improve line of sight to working area.
NVISION BIOMEDICAL TECHNOLOGIES, INC.
EARP-R_001-100
In Commercial Distribution
- 00810135960694 ()
- Self-retaining surgical retractor, reusable
EARP Retractor, EARP BLADE 90.
The EARP Retractor is used in conjunction with TeDan Phantom ML MIS Lumbar Surgical Access System ML-2000 to assist with focal retraction, to increase working corridor and improve line of sight to working area.
NVISION BIOMEDICAL TECHNOLOGIES, INC.
EARP-R_001-90
In Commercial Distribution
- 00810135960687 ()
- Self-retaining surgical retractor, reusable
EARP Retractor, EARP BLADE 80.
The EARP Retractor is used in conjunction with TeDan Phantom ML MIS Lumbar Surgical Access System ML-2000 to assist with focal retraction, to increase working corridor and improve line of sight to working area.
NVISION BIOMEDICAL TECHNOLOGIES, INC.
EARP-R_001-80
In Commercial Distribution
- 00810135960670 ()
- Self-retaining surgical retractor, reusable
EARP Retractor, EARP BLADE 70.
The EARP Retractor is used in conjunction with TeDan Phantom ML MIS Lumbar Surgical Access System ML-2000 to assist with focal retraction, to increase working corridor and improve line of sight to working area.
NVISION BIOMEDICAL TECHNOLOGIES, INC.
EARP-R_001-70
In Commercial Distribution
- 00810135960663 ()
- Self-retaining surgical retractor, reusable