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The API 20 A system enables 21 tests to be carried out for ID of anaerobes. Other tests such as colonial and microscopic morphology, Gram stain, etc. to confirm or complete ID
BIOMERIEUX SA
20300
In Commercial Distribution
- 03573026048150 ()
- Multiple anaerobic bacteria species culture isolate identification IVD, kit
API 20 NE is a standardized system for the ID of non-fastidious, non-enteric Gram-negative rods (e.g. Pseudomonas, Acinetobacter, Flavobacterium, Moraxella, etc.)
BIOMERIEUX SA
20050
In Commercial Distribution
- 03573026047702 ()
- Multiple gram negative bacteria species culture isolate identification IVD, kit
4-hour ID of Enterobacteriaceae. API®strips give accurate ID based on extensive databases and are standardized, easy-to-use test systems.
BIOMERIEUX SA
RAPID 20 E™
In Commercial Distribution
- 03573026048617 ()
- 03573026588526 ()
- Multiple gram negative bacteria species culture isolate identification IVD, kit
API 20 E is a standardized identification system for Enterobacteriaceae and other non-fastidious, Gramnegative rods
BIOMERIEUX SA
API 20 E™
In Commercial Distribution
- 03573026048013 ()
- 03573026588489 ()
- 03573026588496 ()
- 03573026047818 ()
- Multiple gram negative bacteria species culture isolate identification IVD, kit
M4 Valor Wheelchair 20”, Universal armrests, Swing-away Footrests
Drive Devilbiss Healthcare
GVPLA420FBUA RAD-SF
In Commercial Distribution
- 00822383024615 ()
- Push-rim manual wheelchair, bariatric
Content: 20 g Mamelon dark
ZIRKONZAHN SRL
KEAA3801
In Commercial Distribution
- D800KEAA3801 ()
- Dental appliance fabrication material, ceramic
Content: 20 g Mamelon light
ZIRKONZAHN SRL
KEAA3701
In Commercial Distribution
- D800KEAA3701 ()
- Dental appliance fabrication material, ceramic
Content: 20 g Tissue coloured dentine
ZIRKONZAHN SRL
KEAA2001
In Commercial Distribution
- D800KEAA2001 ()
- Dental appliance fabrication material, ceramic
Tinto Cytokeratin 20 is a mouse monoclonal antibody derived from cell culture supernatant that is concentrated, dialyzed, filter sterilized and diluted in buffer pH 7.5
BIO SB, INC.
Predilute, 15 ml
In Commercial Distribution
- B502BSB53880 ()
BSB 5388
- Cytokeratin IVD, antibody
Tinto Cytokeratin 20 is a mouse monoclonal antibody derived from cell culture supernatant that is concentrated, dialyzed, filter sterilized and diluted in buffer pH 7.5
BIO SB, INC.
Predilute, 7 ml
In Commercial Distribution
- B502BSB53870 ()
BSB 5387
- Cytokeratin IVD, antibody
Tinto Cytokeratin 20 is a mouse monoclonal antibody derived from cell culture supernatant that is concentrated, dialyzed, filter sterilized and diluted in buffer pH 7.5
BIO SB, INC.
Predilute, 3 ml
In Commercial Distribution
- B502BSB53860 ()
BSB 5386
- Cytokeratin IVD, antibody
Tinto Cytokeratin 20 is a rabbit monoclonal antibody derived from cell culture supernatant that is concentrated, dialyzed, filter sterilized and diluted in buffer pH 7.5
BIO SB, INC.
Predilute, 15 ml
In Commercial Distribution
- B502BSB67040 ()
BSB 6704
- Cytokeratin IVD, antibody
Tinto Cytokeratin 20 is a rabbit monoclonal antibody derived from cell culture supernatant that is concentrated, dialyzed, filter sterilized and diluted in buffer pH 7.5
BIO SB, INC.
Predilute, 7 ml
In Commercial Distribution
- B502BSB67030 ()
BSB 6703
- Cytokeratin IVD, antibody
Tinto Cytokeratin 20 is a rabbit monoclonal antibody derived from cell culture supernatant that is concentrated, dialyzed, filter sterilized and diluted in buffer pH 7.5
BIO SB, INC.
Predilute, 3 ml
In Commercial Distribution
- B502BSB67020 ()
BSB 6702
- Cytokeratin IVD, antibody
Comfort Band Non-Sterile 20" Green
Tz Medical, Inc.
CB-7520G
In Commercial Distribution
- 00811331011821 ()
- Vascular puncture haemostasis arm clamp/band, single-use
No Description
ELECTRO-CAP INTERNATIONAL INC
I1-3-20ELEC
In Commercial Distribution
- 00811478012569 ()
I1-3-20ELEC
- Analytical scalp lead
No Description
ELECTRO-CAP INTERNATIONAL INC
I1-2-20ELEC
In Commercial Distribution
- 00811478012538 ()
I1-2-20ELEC
- Analytical scalp lead
No Description
ELECTRO-CAP INTERNATIONAL INC
I1-1
In Commercial Distribution
- 00811478012507 ()
I1-1
- Analytical scalp lead
3 units
NUSMILE, LTD.
UDMO2004
In Commercial Distribution
- 00810092938750 ()
- Manual non-rotary dental instrument handle
3 units
NUSMILE, LTD.
UDMS2002
In Commercial Distribution
- 00810092938705 ()
- Manual non-rotary dental instrument handle
Blister of 6 units
NUSMILE, LTD.
ZHEDST3120
In Commercial Distribution
- 00810118100987 ()
- Rotary/reciprocating endodontic file/rasp, single-use
Blister of 6 units
NUSMILE, LTD.
ZHEDST2520
In Commercial Distribution
- 00810118100871 ()
- Rotary/reciprocating endodontic file/rasp, single-use
Blister of 6 units
NUSMILE, LTD.
ZHEDST2120
In Commercial Distribution
- 00810118100765 ()
- Rotary/reciprocating endodontic file/rasp, single-use
Blister of 6 units
NUSMILE, LTD.
ZKFLEX3120
In Commercial Distribution
- 00810118100666 ()
- Rotary/reciprocating endodontic file/rasp, single-use
Blister of 6 units
NUSMILE, LTD.
ZKFLEX2520
In Commercial Distribution
- 00810118100581 ()
- Rotary/reciprocating endodontic file/rasp, single-use
Blister of 6 units
NUSMILE, LTD.
ZKFLEX2120
In Commercial Distribution
- 00810118100505 ()
- Rotary/reciprocating endodontic file/rasp, single-use
Blister of 6 units
NUSMILE, LTD.
ZKFILE3120
In Commercial Distribution
- 00810118100413 ()
- Rotary/reciprocating endodontic file/rasp, single-use
Blister of 6 units
NUSMILE, LTD.
ZKFILE2520
In Commercial Distribution
- 00810118100291 ()
- Rotary/reciprocating endodontic file/rasp, single-use
Blister of 6 units
NUSMILE, LTD.
ZKFILE2120
In Commercial Distribution
- 00810118100178 ()
- Rotary/reciprocating endodontic file/rasp, single-use
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
- 04047844116241 ()
- 17x9x32mm
TRT20170932
- 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
- 04047844115756 ()
- 17x9x28mm
TRT20170928
- 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
- 04047844115275 ()
- 17x9x24mm
TRT20170924
- 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
- 04047844115251 ()
- 15x9x24mm
TRT20150924
- 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
- 04047844115213 ()
- 13x9x24mm
TRT20130924
- 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
- 04047844114766 ()
- 15x9x20mm
TRT20150920
- 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
- 04047844114735 ()
- 12x9x20mm
TRT20120920
- 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
- 04047844116258 ()
- 18x9x32mm
TRT20180932
- 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
- 04047844116234 ()
- 16x9x32mm
TRT20160932
- 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
- 04047844115763 ()
- 18x9x28mm
TRT20180928
- 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
- 04047844115749 ()
- 16x9x28mm
TRT20160928
- Metallic spinal interbody fusion cage