2,200 results
·
50ms
·
Sources: EU EUDAMED, US FDA
BioPlex 2200
FDA UDI
BIO-RAD LABORATORIES, INC.·00847865012508·APLS IgG, IgM and IgA Assay Protocol File CD, S...
BioPlex 2200
FDA UDI
BIO-RAD LABORATORIES, INC.·00847865000604·APLS IgG Reagent Pack
SYSTEMIC LUPUS ERYTHEMATOSUS (SLE)
FDA registration
TECO DIAGNOSTICS·3 products·🇺🇸 United States
Corgenix Anti-Beta-2 Glycoprotein IgA Semi-Quantitative Test Kit
FDA registration
CORGENIX, INC.·3 products·🇺🇸 United States
Stent, Iliac
FDA Pre-Market Approval
FDA Class 3
·PROTEGE GPS CAROTID STENT SYSTEM, PROTEGE GPS SELF-EXPANDING PERIPHERAL STENT SYSTEM
Agent, Bulking, Injectable For Gastro-Urology Use
FDA Pre-Market Approval
FDA Class 3
·MACROPLASTIQUE IMPLANTS, MPQ-2.5
Stent, Iliac
FDA Pre-Market Approval
FDA Class 3
·PROTEGE GPS STENT SYSTEM
Drexco Medical speculum vaginal cusco
Device
EU MDD
·
Eu Md Class 1
·G P S S.R.L. ·On the market·2 countries
Drexco Medical speculum vaginal cusco
Device
EU MDD
·
Eu Md Class 1
·G P S S.R.L. ·On the market·2 countries
drexco medical
Device
EU MDD
·
Eu Md Class 1
·G P S S.R.L. ·On the market·2 countries
drexo medical
Device
EU MDD
·
Eu Md Class 1
·G P S S.R.L. ·On the market·2 countries
DePuy Synthes Porous Polyethylene Implants And Titanium Wires Portfolio MR Conditional
FDA registration
Synthes (USA) Products LLC·2 products·🇺🇸 United States
EliA B2-Glycoprotein I IgG
FDA registration
PHADIA AB·3 products·🇸🇪 Sweden
EliA B2-Glycoprotein I IgG
FDA registration
PHADIA AB·3 products·🇸🇪 Sweden
EliA B2-Glycoprotein I IgG
FDA registration
PHADIA US INC.·3 products·🇺🇸 United States
Sharay Anti-β2-GP1 IgA/G/M (CLIA)
Device
EU IVDD
·
Eu Ivd General
·C-Luminary Biotechnology Co., Ltd.·No longer on the market
BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM-MINOCYCLINE (GP) 1-32 UG/ML
FDA 510(k)
FDA Class 2
·Microbiology
BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM - CEFOXITIN GP 1-32 G/ML
FDA 510(k)
FDA Class 2
·Microbiology
Stent, Carotid
FDA Pre-Market Approval
FDA Class 3
·Protégé GPS and Protégé RX Carotid Stent Systems, and Protégé GPS Peripheral Stent Systems
IMMCO DIAGNOSTICS
FDA UDI
IMMCO DIAGNOSTICS, INC.·00845714004353·Serum Diluent