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The Neuroguard IEP System consists of three main components:
• A self-expanding nitinol stent
• A delivery catheter which includes a post-dilation balloon and activation handle
• Embolic protection filter that is integrated at the distal end of the delivery system
Contego Medical, Inc.
NG-NV-7-30
In Commercial Distribution
- 00851616007637 ()
NG-NV-7-30
- Peripheral angioplasty balloon catheter, basic
- Bare-metal carotid artery stent
- Carotid artery embolic protection system
The Neuroguard IEP System consists of three main components:
• A self-expanding nitinol stent
• A delivery catheter which includes a post-dilation balloon and activation handle
• Embolic protection filter that is integrated at the distal end of the delivery system
Contego Medical, Inc.
NG-NV-7-40
In Commercial Distribution
- 00851616007620 ()
NG-NV-7-40
- Peripheral angioplasty balloon catheter, basic
- Carotid artery embolic protection system
- Bare-metal carotid artery stent
The Neuroguard IEP System consists of three main components:
• A self-expanding nitinol stent
• A delivery catheter which includes a post-dilation balloon and activation handle
• Embolic protection filter that is integrated at the distal end of the delivery system
Contego Medical, Inc.
NG-0740-140-2
In Commercial Distribution
- 00851616007613 ()
NG-0740-140-2
- Peripheral angioplasty balloon catheter, basic
- Bare-metal carotid artery stent
- Carotid artery embolic protection system
The Neuroguard IEP System consists of three main components:
• A self-expanding nitinol stent
• A delivery catheter which includes a post-dilation balloon and activation handle
• Embolic protection filter that is integrated at the distal end of the delivery system
Contego Medical, Inc.
NG-0730-140-2
In Commercial Distribution
- 00851616007606 ()
NG-0730-140-2
- Bare-metal carotid artery stent
- Carotid artery embolic protection system
- Peripheral angioplasty balloon catheter, basic
The Neuroguard IEP System consists of three main components:
• A self-expanding nitinol stent
• A delivery catheter which includes a post-dilation balloon and activation handle
• Embolic protection filter that is integrated at the distal end of the delivery system
Contego Medical, Inc.
NG-0640-140-2
In Commercial Distribution
- 00851616007590 ()
NG-0640-140-2
- Peripheral angioplasty balloon catheter, basic
- Carotid artery embolic protection system
- Bare-metal carotid artery stent
The Neuroguard IEP System consists of three main components:
• A self-expanding nitinol stent
• A delivery catheter which includes a post-dilation balloon and activation handle
• Embolic protection filter that is integrated at the distal end of the delivery system
Contego Medical, Inc.
NG-0630-140-2
In Commercial Distribution
- 00851616007583 ()
NG-0630-140-2
- Bare-metal carotid artery stent
- Carotid artery embolic protection system
- Peripheral angioplasty balloon catheter, basic
Bone level Mini Premill Abutment 14 x 1 mm
"Implant system for the support of dental prostheses, aimed at restoring missing teeth for aesthetical and functional purposes.
Instruments dedicated to implant system for the support of dental prostheses. "
Novodent SA
S-BMPA14
In Commercial Distribution
- 07640168189556 ()
S-BMPA14
- Dental implant suprastructure, permanent, preformed
DISPOSABLE medical devices. Abutment to be screwed into a dental implant. The connection and the thread are compatible with the specific implant; available in different cuff heights. Retentive caps of different retentive forces, metal housing for the caps and protective disc.
RHEIN 83 SRL
S/BLOCK AT STRAUMANN N/NECK ø3,5 h2 TiN
202BFT352R
- Dental implant suprastructure, permanent, preformed
No Description
RHEIN 83 SRL
S/BLOCK AT STRAUMANN N/NECK ø3,5 h2 TiN
Not in Commercial Distribution
- D821202BFT352R0 ()
202BFT352R
- Dental implant suprastructure, permanent, preformed
The CAVUX Cage-LX is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine (C3-C7) with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have received at least six weeks of non-operative treatment prior to treatment with the device. Devices are intended to be used with autogenous bone graft and supplemental fixation, such as an anterior plating system.
Providence Medical Technology, Inc.
PD-31-205
In Commercial Distribution
- 00852776006560 ()
- Implantable cervical facet joint distractor