- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on May 21, 2026
B-6-99B7"REF: USIA00000065M, USIA00000066M" 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-6-99B7"REF: USIA00000065M, USIA00000066M"D-6-99B7
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA / IFA support is coming.
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0102100301THYROID PEROXIDASE (INCL. MICROSOMAL) ANTIBODIESPrimary 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 0020CancelledNotified 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.
View in glossary →B-6-95AXOn the market"REF: U87682040M-2, U87689060M, U87685020M, U87611020M-2, U87620060M-2"B-6-33A9On the market/69357407ICAS000018AZOn the market"REF: USIA00000199M, USIA00000200M"B-6-116FFOn the market"REF: USIA00000219M, USIA00000220M"B-6-125FGOn the market/69357407ICAS000023ASOn the marketNo certificate specifically references this device's Basic UDI-DI.