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VitriFit™

EUDAMED

Class IIa (EU MDR)

Ref 42792001

by CooperSurgical, Inc.

Identity

Trade Name
VitriFit™ EUDAMED
Device Name
VitriFit™ EUDAMED
Model / Reference
42792001 EUDAMED

Identifiers

Primary DI / UDI-DI
20888937028786 EUDAMED
Basic UDI-DI
0888937TD044ZP EUDAMED
Direct Marketing DI
20888937028786 EUDAMED
EMDN Code
U08020401 CRYOPRESERVATION CONTAINERS/STRAWS/VIALS FOR ASSISTED REPRODUCTION EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

VitriFit™ by CooperSurgical, Inc. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
US-MF-000002607
Authorised Representative
CooperSurgical Distribution B.V. NL-AR-000000059

Sources (1)

  • EUDAMED a2ad8947-6004-461c-a6ab-9a057226ea5a 61 fields · synced Jun 19, 2026