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EmbryoScope 8

by Vitrolife A/S 2 variants

Ref 16409

EmbryoScope 8 (16409) is a medical device (EU MDR Class IIa; EMDN category devices for assisted reproduction) made by Vitrolife A/S, registered in EUDAMED on 7 Dec 2022 (Basic UDI-DI 5712714INC-01KD), active as of 23 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5712714INC-01KD Basic UDI-DI 05712714604096UDI-DIDate7 Dec 2022RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
EmbryoScope+
Model / reference
16409
Primary DI / UDI-DI
05712714604096
Basic UDI-DI
5712714INC-01KD
Direct marketing DI
05712714604096
EMDN code
U080299 Devices for assisted reproduction - other
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Denmark

Manufacturer details

EUDAMED SRN
DK-MF-000001892

Similar devices in this category

Other devices filed under DEVICES FOR ASSISTED REPRODUCTION - OTHER.

Other devices from Vitrolife A/S

See all devices from Vitrolife A/S →

Properties

Other properties (14, all answered No)