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UDI Compass

VITROS™ ECL SHBG Assay

No Certificate Found

Snapshot 2026-11-02 · Link to EUDAMED

UDI-DI 06978139076781Basic UDI-DI 69703416803205096K2

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Class B · IVDR · Shenzhen Lifotronic Technology Co., Ltd.

Identification

Model
50T，2×50T，100T，2×100T
Issuing agency
GS1
Device status
active
Sterile
No

Certificates

No certificate found.

Snapshot 2026-11-02 · Link to EUDAMED

Manufacturer

Shenzhen Lifotronic Technology Co., Ltd.

SRN CN-MF-000005654

CN · Shenzhen

manufacturer

Authorised representative: Shanghai International Holding Corp. GmbH(Europe) (DE-AR-000000001)

Related UDI-DIs

NameUDI-DICertificate
SHBG (eCLIA)06975984063690
No Certificate Found

Snapshot 2026-11-02 · Link to EUDAMED

SHBG (eCLIA)06975984063706
No Certificate Found

Snapshot 2026-11-02 · Link to EUDAMED

All UDI-DIs in this Basic UDI-DI family

Canonical device page: /device/vitrostm-ecl-shbg-assay-6781 · UDI page: /udi/06978139076781

All devices from Shenzhen Lifotronic Technology Co., Ltd.