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UDI Compass
Certificate valid

Snapshot 2026-10-10 · Link to EUDAMED

Cryotec

UDI-DI 04589700011012Basic UDI-DI 458970001TECND

Class IIa · MDR · REPROLIFE Inc.

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

4203458CE01

EU quality management system · valid

Notified body: DEKRA Certification B.V. (0344)

Valid from 2026-07-17 · Expiry 2031-07-01

Scope not stated in certificate data.

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

Manufacturer

REPROLIFE Inc.

SRN JP-MF-000031415

JP · Shinjuku-ku, Tokyo

manufacturer

Authorised representative: Medical Technology Promedt Consulting GmbH (DE-AR-000000085)

Related UDI-DIs

All UDI-DIs in this Basic UDI-DI family

Canonical device page: /device/cryotec-1012 · UDI page: /udi/04589700011012

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