Skip to content

Acriva

by VSY Biotechnology GmbH 1,000+ variants

Ref ACRIVA UD 613

Acriva (ACRIVA UD 613) is a Class IIb device made by VSY Biotechnology GmbH, registered in EUDAMED on 4 Aug 2026 (Basic UDI-DI B-04064544240168), active as of 24 Oct 2026.

Active European Union

CE MDD

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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-04064544240168 Basic UDI-DI Date4 Aug 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Acriva Ud 613
Model / reference
ACRIVA UD 613
Primary DI / UDI-DI
04064544240168, 04064544241301, 04064544240205, 04064544241325, 04064544241462, 04064544240601, 04064544241370, 04064544240465, 04064544239971, 04064544240069, 04064544240434, 04064544241400, 04064544239827, 04064544240199, 04064544241332, 04064544241387, 04064544240557, 04064544240311, 04064544240151, 04064544240489, 04064544241240, 04064544239865, 04064544241264, 04064544240076, 04064544240267, 04064544241271, 04064544239926, 04064544240496, 04064544240106, 04064544239742, 04064544240090, 04064544240564, 04064544240571, 04064544239902, 04064544239896, 04064544240045, 04064544239933, 04064544240519, 04064544239834, 04064544239810, 04064544241295, 04064544240632, 04064544240120, 04064544240304, 04064544240533, 04064544239988, 04064544241509, 04064544240014, 04064544241318, 04064544240373
Basic UDI-DI
B-04064544240168, B-04064544241301, B-04064544240205, B-04064544241325, B-04064544241462, B-04064544240601, B-04064544241370, B-04064544240465, B-04064544239971, B-04064544240069, B-04064544240434, B-04064544241400, B-04064544239827, B-04064544240199, B-04064544241332, B-04064544241387, B-04064544240557, B-04064544240311, B-04064544240151, B-04064544240489, B-04064544241240, B-04064544239865, B-04064544241264, B-04064544240076, B-04064544240267, B-04064544241271, B-04064544239926, B-04064544240496, B-04064544240106, B-04064544239742, B-04064544240090, B-04064544240564, B-04064544240571, B-04064544239902, B-04064544239896, B-04064544240045, B-04064544239933, B-04064544240519, B-04064544239834, B-04064544239810, B-04064544241295, B-04064544240632, B-04064544240120, B-04064544240304, B-04064544240533, B-04064544239988, B-04064544241509, B-04064544240014, B-04064544241318, B-04064544240373
EMDN code
P030102090202 IOLs, APHAKIC, MONOFOCAL, ASPHERIC, HYDROPHILIC ACRYLIC
Device class
Class IIb
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000025210

Similar devices in this category

Other devices filed under IOLs, APHAKIC, MONOFOCAL, ASPHERIC, HYDROPHILIC ACRYLIC.

Other devices from VSY Biotechnology GmbH

See all devices from VSY Biotechnology GmbH →

Properties

  • Supplied sterile
  • Implantable
Other properties (12, all answered No)