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