10,000 results
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397ms
·
Sources: EU EUDAMED, US FDA
Hemagard
FDA UDI
INTERVASCULAR SAS·00384401014171·Hemagard Knitted Straight Radially Supported Co...
SEEQ™
FDA UDI
MEDTRONIC, INC.·00763000065744·EXT CARDIAC SEEQ14 4WK KIT US PHAR TUV
Dynaflo® Bypass Grafts
FDA UDI
Bard Peripheral Vascular, Inc.·00801741023736·Dynaflo® Bypass Graft With Flex Small Beading, ...
Intergard
FDA UDI
INTERVASCULAR SAS·00384401000952·Intergard Knitted Straight Collagen Coated Vasc...
Hemagard
FDA UDI
INTERVASCULAR SAS·00384401014317·Hemagard Knitted Straight Collagen Coated Vascu...
SealPTFE™
FDA UDI
VASCUTEK LTD·05037881152783·SEALPTFE Gelatin Sealed ePTFE Vascular Prosthes...
AVANOS
FDA UDI
Avanos Medical, Inc.·00609038993270·BALLARD* Endotracheal Tube Adapter
Gelweave™
FDA UDI
VASCUTEK LTD·05037881998527·Gelweave Gelatin Impregnated Woven Vascular Pro...
SealPTFE™
FDA UDI
VASCUTEK LTD·05037881152363·SEALPTFE Gelatin Sealed ePTFE Vascular Prosthes...
SealPTFE™
FDA UDI
VASCUTEK LTD·05037881152776·SEALPTFE Gelatin Sealed ePTFE Vascular Prosthes...
Centurion
FDA UDI
CENTURION MEDICAL PRODUCTS CORPORATION·00653160019902·MUCUS TRAP W/GLOVES 14 FR
BioPlex 2200 APLS IgG and IgA kit
FDA registration
Bio-Rad Laboratories, Inc.·4 products·🇺🇸 United States
BioPlex 2200 APLS IgM
FDA registration
Bio-Rad Laboratories, Inc.·4 products·🇺🇸 United States
BioPlex2200 APLS IgA Reagent Pack
FDA registration
BIO-RAD LABORATORIES, INC.·4 products·🇺🇸 United States
BioPlex2200 APLS IgM Control Set
FDA registration
BIO-RAD LABORATORIES, INC.·4 products·🇺🇸 United States
Circle Cardiovascular Imaging Inc
Manufacturer
🇨🇦 Canada·6 Basic UDI-DIs·7 Devices·3 Importers·BSI Group The Netherlands B.V., SGS Belgium NV, and BSI Group The Netherlands B.V.
ASI RPR Test for Syphilis for Use on the ASI Evolution
FDA UDI
ARLINGTON SCIENTIFIC, INC.·00816057021673·Syphilis Screening Test for Use on the ASI Evol...
ASI RPR Test for Syphilis for Use on the ASI Evolution
FDA UDI
ARLINGTON SCIENTIFIC, INC.·00816057021680·Syphilis Screening Test for Use on the ASI Evol...
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·ENDOTAK RELIANCE G/SG with 4-SITE Connector Defibrillation Leads, Passive Fixation Lead Models: 0265, 0266, 0282, 0283
ASI Toxoplasma IgM EIA Test
FDA UDI
ARLINGTON SCIENTIFIC, INC.·00816057020546·Detection of Toxoplasma Antibody