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VitriFit™

by CooperSurgical, Inc. 11 variants

Part of a family of 11 devices: see the family page

Ref 42825005

VitriFit™ (42825005) is a Class IIa device made by CooperSurgical, Inc., registered in EUDAMED on 13 Jan 2026 (Basic UDI-DI 0888937TD044ZP), 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 Number0888937TD044ZP Basic UDI-DI 20888937028892UDI-DIDate13 Jan 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
42825005
Primary DI / UDI-DI
20888937028892
Basic UDI-DI
0888937TD044ZP
Direct marketing DI
20888937028892
EMDN code
U08020401 Cryopreservation containers/straws/vials for assisted reproduction
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Netherlands

Manufacturer details

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

Similar devices in this category

Other devices filed under CRYOPRESERVATION CONTAINERS/STRAWS/VIALS FOR ASSISTED REPRODUCTION.

Other devices from CooperSurgical, Inc.

See all devices from CooperSurgical, Inc. →

Properties

  • Supplied sterile
Other properties (13, all answered No)