SEARCH RESULTS FOR: Origin(1849 results)
Gelsoft Gelatin Impregnated Knitted Cardiovascular Patch
VASCUTEK LTD
960603
In Commercial Distribution
- 05037881010632 ()
- Dimensions 6 x 3 cm
960603
- Cardiovascular patch, animal-derived
Gelsoft Gelatin Impregnated Knitted Cardiovascular Patch
VASCUTEK LTD
960501
In Commercial Distribution
- 05037881010625 ()
- Dimensions 5 x 1.5 cm
960501
- Cardiovascular patch, animal-derived
Gelsoft Gelatin Impregnated Knitted Cardiovascular Patch
VASCUTEK LTD
960501S
In Commercial Distribution
- 05037881010618 ()
- Dimensions 5 x 1 cm
960501S
- Cardiovascular patch, animal-derived
Gelseal Gelatin Impregnated Knitted Cardiovascular Patch
VASCUTEK LTD
951220
In Commercial Distribution
- 05037881010465 ()
- Dimensions 12 x 20 cm
951220
- Cardiovascular patch, animal-derived
Gelseal Gelatin Impregnated Knitted Cardiovascular Patch
VASCUTEK LTD
951208
In Commercial Distribution
- 05037881010458 ()
- Dimensions 12 x 8 cm
951208
- Cardiovascular patch, animal-derived
Gelseal Gelatin Impregnated Knitted Cardiovascular Patch
VASCUTEK LTD
951204
In Commercial Distribution
- 05037881010441 ()
- Dimensions 12 x 4 cm
951204
- Cardiovascular patch, animal-derived
Gelseal Gelatin Impregnated Knitted Cardiovascular Patch
VASCUTEK LTD
951020
In Commercial Distribution
- 05037881010434 ()
- Dimensions 10 x 20 cm
951020
- Cardiovascular patch, animal-derived
Gelseal Gelatin Impregnated Knitted Cardiovascular Patch
VASCUTEK LTD
951010
In Commercial Distribution
- 05037881010427 ()
- Dimensions 10 x 10 cm
951010
- Cardiovascular patch, animal-derived
Gelseal Gelatin Impregnated Knitted Cardiovascular Patch
VASCUTEK LTD
950804
In Commercial Distribution
- 05037881010410 ()
- Dimensions 8 x 4 cm
950804
- Cardiovascular patch, animal-derived
Magnetic remote control for operation of inFlow urinary prosthesis. With base station and recharger.
VESIFLO INC
Sep 2016
Not in Commercial Distribution
- 08625630003010 ()
403507
- Intraurethral valve/pump
Magnetic remote control for operation of inFlow urinary prosthesis. With base station and recharger.
VESIFLO INC
Sep 2016
Not in Commercial Distribution
- 08625630003001 ()
403507
- Intraurethral valve/pump
Magnetic shield for the inFlow Activator
VESIFLO INC
August 2021
In Commercial Distribution
- 00862563003191 ()
403350
- Intraurethral valve/pump
Magnetic remote control for the inFlow Device
- with base station and medical charger
VESIFLO INC
August 2021
In Commercial Distribution
- 00862563003184 ()
403507K
- Intraurethral valve/pump
Recharger for inFlow Activator
VESIFLO INC
August 2021
In Commercial Distribution
- 00862563003177 ()
403320
- Intraurethral valve/pump
Unit for storing and recharging the inFlow Activator
VESIFLO INC
August 2021
In Commercial Distribution
- 00862563003160 ()
403310
- Intraurethral valve/pump
Magnetic remote control for the inFlow Device
VESIFLO INC
August 2021
In Commercial Distribution
- 00862563003153 ()
403300
- Intraurethral valve/pump
The Atalante X by Wandercraft is a completely self-balancing walking system for people with mobility disabilities. It is a fully powered hip-knee-ankle lower body exoskeleton with 12 actuated degrees of freedom. Atalante X is self-balancing and includes dynamic-walking control. Dynamic walking allows the Atalante X to consume significantly less power and have a more natural gait. The Atalante X is a tool for physical therapy.
It is meant to be highly adjustable and be applicable for various stages of physical rehabilitation, re-mobilization and exercises.
WANDERCRAFT
ATA-002-EN US
In Commercial Distribution
- 03665965000129 ()
- Programmable ambulation exoskeleton, clinical
primaLOK SP 10mm Implant Assembly, Sterile
The Wenzel Spine primaLOK SP Interspinous Fusion System is a posterior, nonpedicle supplemental fixation device, intended for use in the non-cervical spine (T1-S1). it is intended for plate fixation/attachment to spinous process for the purpose of achieving supplemental fusion in the following conditions: degenerative disc disease (defined as ack pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e. fracture or dislocation), and/or tumor. The primaLOK SP Interspinous Fusion System is intended for use at one level with bone graft material and not intended for stand-alone use.
Wenzel Spine, Inc.
800-0110-00
In Commercial Distribution
- 00813210021747 ()
- Height: 10 Millimeter
- Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial
primaLOK SP 8mm Implant Assembly, Sterile
The Wenzel Spine primaLOK SP Interspinous Fusion System is a posterior, nonpedicle supplemental fixation device, intended for use in the non-cervical spine (T1-S1). it is intended for plate fixation/attachment to spinous process for the purpose of achieving supplemental fusion in the following conditions: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e. fracture or dislocation), and/or tumor. The primaLOK SP Interspinous Fusion System is intended for use at one level with bone graft material and not intended for stand-alone use.
Wenzel Spine, Inc.
800-0108-00
In Commercial Distribution
- 00813210021730 ()
- Height: 8 Millimeter
- Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial
The Wenzel Spine VariLift Lumbar Interbody Fusion Device is a self-tapping, expandable device with an interior sliding wedge and a posterior end cap. The VariLift-L is a grooved and fluted device with large graft windows positioned each of its four quadrants that provide bony contact with the endplates. VariLift-L is designed to be implanted bi-laterally via posterior (PLIF) approach or as a single device via a transverse (TLIF) approach. VariLift-L may be implanted with or without supplemental fixation and is intended for use with autograft to facilitate fusion. VariLift-L is indicated for intervertebral body fusion of the lumbar spine, from L2 to S1, in skeletally mature patients who have had six months of non-operative treatment. The device is intended for use at either one level or two contiguous levels for the treatment of degenerative disc disease (DDD) with up to Grade 1 spondylolisthesis. DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies.
Wenzel Spine, Inc.
CIE2-11-24-00
In Commercial Distribution
- 00813210020009 ()
- Length: 24 Millimeter
- Outer Diameter: 11 Millimeter
- Metallic spinal interbody fusion cage