10,000 results
·
48ms
·
Sources: EU EUDAMED, US FDA
MEDI J Co., Ltd
Manufacturer
🇰🇷 South Korea·2 Basic UDI-DIs·2 Devices·POLSKIE CENTRUM BADAN I CERTYFIKACJI S.A.
STA - Reptilase
FDA registration
Diagnostica Stago - Taverny·1 product·🇫🇷 France
STA - Reptilase
FDA registration
DIAGNOSTICA STAGO, INC.·1 product·🇺🇸 United States
Batroxobin Reagent
FDA registration
Siemens Healthcare Diagnostics Products GmbH·1 product·🇩🇪 Germany
STA - Reptilase
FDA registration
Diagnostica Stago - Taverny·1 product·🇫🇷 France
STA® - Reptilase®
FDA UDI
DIAGNOSTICA STAGO·13607450006145·
Batroxobin Reagent
FDA UDI
Siemens Healthcare Diagnostics Products GmbH·00842768011504·Determination of batroxobin time
HYCOGEL
Device
EU MDD
·
Eu Md Class 3
·MEDI J Co., Ltd·On the market·1 country
HYCOGEL
Device
EU MDD
·
Eu Md Class 3
·MEDI J Co., Ltd·On the market·1 country
REPTILASE -PC
FDA 510(k)
FDA Class 2
·Hematology
ATROXIN
FDA 510(k)
FDA Class 2
·Hematology
VENOM TIEM REAGENT
FDA 510(k)
FDA Class 2
·Hematology
BATROXOBIN REAGENT
FDA 510(k)
FDA Class 2
·Hematology
FDP COLLECTION TUBES
FDA 510(k)
FDA Class 2
·Hematology
DUPONT ACA FIBRIN DEGRADATION PROD CLOTTING TUBE
FDA 510(k)
FDA Class 2
·Hematology
REPTILASE-R HA35
FDA 510(k)
FDA Class 2
·Hematology
HYCOGEL
Basic UDI-DI
EU MDD
·
Eu Md Class 3
·MEDI J Co., Ltd·1 device
HYCOGEL
Basic UDI-DI
EU MDD
·
Eu Md Class 3
·MEDI J Co., Ltd·1 device
1434-MDD-070/2021
Certificate
MDD Annex II (excluding section 4)·MEDI J Co., Ltd·POLSKIE CENTRUM BADAN I CERTYFIKACJI S.A.·2 Basic UDI-DIs
Bothrops Atrox Reagent
FDA classification
FDA Class 2
·Bothrops Atrox Reagent