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Emergency Room 13 Test Panel

Devices (same UDI-DI)
1
Certificates
0
Countries
0
Notified Bodies
0

Basic Information

Primary DI
06975838800662
Basic UDI-DI Code
B-06975838800662
Reference
HE50064
Device Types
Single use
Regulation
Eu Ivdd
Classification
Eu Ivd General
Status
On The Market

Additional Description

The Emergency Room 13 Test Panel is intended for in vitro quantitative detection of the concentration or activity of Aspartate Aminotransferase (AST), Uric Acid (UA), Creatinine (CRE), Glucose (GLU), Creatine Kinase (CK), Creatine Kinase Isoenzyme (CK-MB), Lactate Dehydrogenase (LDH), α-Hydroxybutyrate Dehydrogenase (α-HBDH), Amylase (AMY), Potassium Ion (K+), Sodium Ion (Na+), Chloride Ion (CL-), Carbon Dioxide (CO2) in human serum, plasma, whole blood and capillary blood by the microfluidic dry chemistry.

CND Nomenclature Codes

Code Description
W01010404 MULTIPLE PARAMETERS (MIX OF ALL) - CLIN. CHEM LAB R.

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