SEARCH RESULTS FOR: (*Make St Mary*)(21162 results)
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Glaucoma shunt
NEW WORLD MEDICAL, INCORPORATED
ST350
In Commercial Distribution
- 00892064002096 ()
- Area/Surface Area: 350 Square millimeter
10-0610
- Glaucoma shunt, tubular, non-animal-derived
Glaucoma shunt
NEW WORLD MEDICAL, INCORPORATED
ST250
In Commercial Distribution
- 00892064002089 ()
- Area/Surface Area: 250 Square millimeter
10-0609
- Glaucoma shunt, tubular, non-animal-derived
Ablation Catheter
BOSTON SCIENTIFIC CORPORATION
M004R5031TH0
In Commercial Distribution
- 08714729963974 ()
- 7 F Diameter
- 2.33 mm Diameter
- 4 mm Length
M004R5031TH0
- Cardiac radio-frequency ablation system catheter
Ablation Catheter
BOSTON SCIENTIFIC CORPORATION
M004R5031THK20
In Commercial Distribution
- 08714729963950 ()
- 2.33 mm Diameter
- 7 F Diameter
- 4 mm Length
M004R5031THK20
- Cardiac radio-frequency ablation system catheter
Bidirectional Steerable Diagnostic Catheter
BOSTON SCIENTIFIC CORPORATION
M0043200100
Not in Commercial Distribution
- 08714729877851 ()
- 7 F Diameter
- 2.33 mm Diameter
- Cardiac mapping catheter, percutaneous, single-use
Bidirectional Steerable Diagnostic Catheter
BOSTON SCIENTIFIC CORPORATION
M0043200090
Not in Commercial Distribution
- 08714729877844 ()
- 2.33 mm Diameter
- 7 F Diameter
- Cardiac mapping catheter, percutaneous, single-use
Bidirectional Steerable Diagnostic Catheter
BOSTON SCIENTIFIC CORPORATION
M0043200080
Not in Commercial Distribution
- 08714729877837 ()
- 2.33 mm Diameter
- 7 F Diameter
- Cardiac mapping catheter, percutaneous, single-use
Bidirectional Steerable Diagnostic Catheter
BOSTON SCIENTIFIC CORPORATION
M0043200070
Not in Commercial Distribution
- 08714729877820 ()
- 2.33 mm Diameter
- 7 F Diameter
- Cardiac mapping catheter, percutaneous, single-use
Bidirectional Steerable Diagnostic Catheter
BOSTON SCIENTIFIC CORPORATION
M0043200060
Not in Commercial Distribution
- 08714729877813 ()
- 2.33 mm Diameter
- 7 F Diameter
- Cardiac mapping catheter, percutaneous, single-use
Bidirectional Steerable Diagnostic Catheter
BOSTON SCIENTIFIC CORPORATION
M0043200050
Not in Commercial Distribution
- 08714729877806 ()
- 7 F Diameter
- 2.33 mm Diameter
- Cardiac mapping catheter, percutaneous, single-use
Bidirectional Steerable Diagnostic Catheter
BOSTON SCIENTIFIC CORPORATION
M0043200030
Not in Commercial Distribution
- 08714729877783 ()
- 2.33 mm Diameter
- 7 F Diameter
- Cardiac mapping catheter, percutaneous, single-use
Bidirectional Steerable Diagnostic Catheter
BOSTON SCIENTIFIC CORPORATION
M0043200020
Not in Commercial Distribution
- 08714729877776 ()
- 2.33 mm Diameter
- 7 F Diameter
- Cardiac mapping catheter, percutaneous, single-use
Bidirectional Steerable Diagnostic Catheter
BOSTON SCIENTIFIC CORPORATION
M0043200010
Not in Commercial Distribution
- 08714729877769 ()
- 2.33 mm Diameter
- 7 F Diameter
- Cardiac mapping catheter, percutaneous, single-use
70cm 8 Contact Trial Lead Kit
BOSTON SCIENTIFIC NEUROMODULATION CORPORATION
SC-2218-70E
In Commercial Distribution
- 08714729820741 ()
- 70 cm Length
- Implantable electrical stimulation system intraoperative test lead
30cm 8 Contact Lead Kit
BOSTON SCIENTIFIC NEUROMODULATION CORPORATION
SC-2218-30
In Commercial Distribution
- 08714729771180 ()
- 30 cm Length
- Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection
50cm 8 Contact Lead Kit
BOSTON SCIENTIFIC NEUROMODULATION CORPORATION
SC-2218-50
In Commercial Distribution
- 08714729767725 ()
- 50 cm Length
- Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection
70cm 8 Contact Lead Kit
BOSTON SCIENTIFIC NEUROMODULATION CORPORATION
SC-2218-70
In Commercial Distribution
- 08714729767749 ()
- 70 cm Length
- Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection
St. Jude Medical Probe Covers Clear Polyethylene Non-Sterile 9in x 96in x 1in 100 per Case
TIDI PRODUCTS, LLC
33431
Not in Commercial Distribution
- 01618125183882 ()
- Medical equipment/instrument drape, single-use
St. Jude Medical Probe Covers Clear Polyethylene Sterile 9in x 96in x 1in 100 per Case
TIDI PRODUCTS, LLC
30965
Not in Commercial Distribution
- 00618125167883 ()
- 01618125167882 ()
- Medical equipment/instrument drape, single-use
50cm 8 Contact Trial Lead Kit
BOSTON SCIENTIFIC NEUROMODULATION CORPORATION
SC-2218-50E
In Commercial Distribution
- 08714729784067 ()
- 50 cm Length
- Implantable electrical stimulation system intraoperative test lead
No Description
DENTAL MANUFACTURING SPA
EVO 2 ST 8 LOWER
Not in Commercial Distribution
- 28056865012906 ()
- 08056865012834 ()
- 28056865012838 ()
0120083
- Resin artificial teeth
No Description
DENTAL MANUFACTURING SPA
EVO 2 ST 8 UPPER
Not in Commercial Distribution
- 28056865012906 ()
- 08056865012827 ()
- 28056865012821 ()
0120082
- Resin artificial teeth
No Description
DENTAL MANUFACTURING SPA
EVO 2 ST 6 LOWER
Not in Commercial Distribution
- 28056865012906 ()
- 08056865012810 ()
- 18056865012817 ()
0120081
- Resin artificial teeth
No Description
DENTAL MANUFACTURING SPA
EVO 2 ST 6 UPPER
Not in Commercial Distribution
- 08056865012803 ()
- 28056865012906 ()
- 18056865012800 ()
0120080
- Resin artificial teeth
The SIGNUS TETRIS™ ST and SIGNUS TETRIS™ R ST system is an intervertebral fusion device to treat degenerative disc disease. The implants are additively manufactured from titanium alloy (Ti-6Al-4V). Each device is available in a single footprint, with multiple heights and angulations. The SIGNUS TETRIS™ ST/ TETRIS™ R ST device is placed by a PLIF (Posterior Lumbar Interbody Fusion) approach in the L2 – S1 spinal region and should be inserted in pairs. The device is comprised of structural titanium in an open-pore grid structure. The large fenestration in the implant permits the cage to be packed with autogenous bone graft and/or allograft comprised of cancellous and/or corticocancellous bone graft to facilitate fusion.
SIGNUS Medizintechnik GmbH
Lumbar cage, angled
In Commercial Distribution
- 04047844114230 ()
- 15x10x32mm
TST20151032
- Metallic spinal interbody fusion cage
The SIGNUS TETRIS™ ST and SIGNUS TETRIS™ R ST system is an intervertebral fusion device to treat degenerative disc disease. The implants are additively manufactured from titanium alloy (Ti-6Al-4V). Each device is available in a single footprint, with multiple heights and angulations. The SIGNUS TETRIS™ ST/ TETRIS™ R ST device is placed by a PLIF (Posterior Lumbar Interbody Fusion) approach in the L2 – S1 spinal region and should be inserted in pairs. The device is comprised of structural titanium in an open-pore grid structure. The large fenestration in the implant permits the cage to be packed with autogenous bone graft and/or allograft comprised of cancellous and/or corticocancellous bone graft to facilitate fusion.
SIGNUS Medizintechnik GmbH
Lumbar cage, angled
In Commercial Distribution
- 04047844114179 ()
- 18x10x32mm
TST16181032
- Metallic spinal interbody fusion cage
The SIGNUS TETRIS™ ST and SIGNUS TETRIS™ R ST system is an intervertebral fusion device to treat degenerative disc disease. The implants are additively manufactured from titanium alloy (Ti-6Al-4V). Each device is available in a single footprint, with multiple heights and angulations. The SIGNUS TETRIS™ ST/ TETRIS™ R ST device is placed by a PLIF (Posterior Lumbar Interbody Fusion) approach in the L2 – S1 spinal region and should be inserted in pairs. The device is comprised of structural titanium in an open-pore grid structure. The large fenestration in the implant permits the cage to be packed with autogenous bone graft and/or allograft comprised of cancellous and/or corticocancellous bone graft to facilitate fusion.
SIGNUS Medizintechnik GmbH
Lumbar cage, angled
In Commercial Distribution
- 04047844114148 ()
- 15x10x32mm
TST16151032
- Metallic spinal interbody fusion cage
The SIGNUS TETRIS™ ST and SIGNUS TETRIS™ R ST system is an intervertebral fusion device to treat degenerative disc disease. The implants are additively manufactured from titanium alloy (Ti-6Al-4V). Each device is available in a single footprint, with multiple heights and angulations. The SIGNUS TETRIS™ ST/ TETRIS™ R ST device is placed by a PLIF (Posterior Lumbar Interbody Fusion) approach in the L2 – S1 spinal region and should be inserted in pairs. The device is comprised of structural titanium in an open-pore grid structure. The large fenestration in the implant permits the cage to be packed with autogenous bone graft and/or allograft comprised of cancellous and/or corticocancellous bone graft to facilitate fusion.
SIGNUS Medizintechnik GmbH
Lumbar cage, angled
In Commercial Distribution
- 04047844114131 ()
- 17x10x32mm
TST16171032
- Metallic spinal interbody fusion cage
The SIGNUS TETRIS™ ST and SIGNUS TETRIS™ R ST system is an intervertebral fusion device to treat degenerative disc disease. The implants are additively manufactured from titanium alloy (Ti-6Al-4V). Each device is available in a single footprint, with multiple heights and angulations. The SIGNUS TETRIS™ ST/ TETRIS™ R ST device is placed by a PLIF (Posterior Lumbar Interbody Fusion) approach in the L2 – S1 spinal region and should be inserted in pairs. The device is comprised of structural titanium in an open-pore grid structure. The large fenestration in the implant permits the cage to be packed with autogenous bone graft and/or allograft comprised of cancellous and/or corticocancellous bone graft to facilitate fusion.
SIGNUS Medizintechnik GmbH
Lumbar cage, angled
In Commercial Distribution
- 04047844114087 ()
- 17x10x32mm
TST12171032
- Metallic spinal interbody fusion cage
The SIGNUS TETRIS™ ST and SIGNUS TETRIS™ R ST system is an intervertebral fusion device to treat degenerative disc disease. The implants are additively manufactured from titanium alloy (Ti-6Al-4V). Each device is available in a single footprint, with multiple heights and angulations. The SIGNUS TETRIS™ ST/ TETRIS™ R ST device is placed by a PLIF (Posterior Lumbar Interbody Fusion) approach in the L2 – S1 spinal region and should be inserted in pairs. The device is comprised of structural titanium in an open-pore grid structure. The large fenestration in the implant permits the cage to be packed with autogenous bone graft and/or allograft comprised of cancellous and/or corticocancellous bone graft to facilitate fusion.
SIGNUS Medizintechnik GmbH
Lumbar cage, angled
In Commercial Distribution
- 04047844114070 ()
- 16x10x32mm
TST12161032
- Metallic spinal interbody fusion cage