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EUDAMED last updated this device on May 21, 2026
B-6-90AM"REF: USIA00000075M, USIA00000076M" is an IVDD-legacy in vitro diagnostic registered in EUDAMED. It is classified as IVDD — General. Manufactured by URIT Medical Electronic Co.,Ltd.. Placed on the EU market in Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
D-6-90AM"REF: USIA00000075M, USIA00000076M"D-6-90AM
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.
European Medical Device Nomenclature — the EU product classification assigned to this device.
W01010115CREATINE KINASE ISOENZYMESPrimary placement in Spain; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| SpainPrimary placement | — | Still on market |
CN-MF-000011840Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
View in glossary →Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →IVDR risk classes
IVDR risk classes rank in-vitro diagnostic devices from lowest risk (Class A) to highest (Class D), based on the patient and public-health risk of a wrong result.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Certificate health across this manufacturer's portfolio.
G10 074544 0020IssuedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
B-6-119FMOn the market"REF: USCA00000623 USCA00000783 USCA00000784 USCA00000785 USCA00000786 USCA00000787 USCA00000788 USCA00000789"B-6-137FPOn the market"REF: USIA00000069M, USIA00000070M"B-6-83AQOn the market"REF: USIA00000145M, USIA00000146M"B-6-80AJOn the market"REF: USIA00000209M, USIA00000210M"B-6-122FAOn the market"REF: U88082040M, U88089040M, U88085020M, U88011020M, U88020040M"B-6-43ACOn the marketNo certificate specifically references this device's Basic UDI-DI.