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EmbryoScope

EUDAMED

Class IIa (EU MDR)

Ref ESD20000-JAP

by Vitrolife A/S

Identity

Trade Name
EmbryoScope EUDAMED
Device Name
EmbryoScope EUDAMED
Model / Reference
ESD20000-JAP EUDAMED

Identifiers

Primary DI / UDI-DI
05712714603037 EUDAMED
Basic UDI-DI
5712714INC-02KF EUDAMED
Direct Marketing DI
05712714603037 EUDAMED
EMDN Code
U080299 DEVICES FOR ASSISTED REPRODUCTION - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Denmark EUDAMED

Clinical & Handling

Sterile

No

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

Category: Assisted reproduction vitrification carrier

EmbryoScope by Vitrolife A/S — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Assisted reproduction vitrification carrier.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Vitrolife A/S
EUDAMED SRN
DK-MF-000001892

Sources (1)

  • EUDAMED 278b1c36-6d1d-4538-a146-5de2c81c24de 61 fields · synced Jun 18, 2026