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UDI Compass
Certificate valid

Snapshot 2026-10-10 · Link to EUDAMED

LiquID 071

UDI-DI 00850012180012Basic UDI-DI 0850012180M20007F5F

Class III · MDR · Seigla Medical, Inc.

Identification
Model
—
Issuing agency
GS1
Device status
active
Sterile
Yes
Implantable
No
Measuring function
No
Reusable surgical
No
Certificates

28620207793

EU technical documentation assessment · valid

Notified body: Intertek Medical Notified Body AB (2862)

Valid from 2025-03-17 · Expiry 2029-12-01

Scope not stated in certificate data.

Certificate’s own scope text — not a compliance opinion from UDI Compass.

Manufacturer

Seigla Medical, Inc.

SRN US-MF-000032398

US · Buffalo

manufacturer

Authorised representative: MDSS GmbH (DE-AR-000005430)

Related UDI-DIs

No other UDI-DIs share this Basic UDI-DI in this snapshot.

All UDI-DIs in this Basic UDI-DI family

Canonical device page: /device/liquid-071-0012 · UDI page: /udi/00850012180012

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