Skip to content

BIOVITEX -RESTORING FLUID - 5+5 (1+1x500 mL T)

by Biolife Italiana s.r.l.

Ref 4240009Model ADDITIVES FOR CULTURE MEDIA

Active European Union

CE IVDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number805645050SUPPLEMENTS042E9 Basic UDI-DI 08056450503273UDI-DIDate8 Jul 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Active

Specification

EUDAMED

Device Name
Additives for Culture Media
Model / Reference
ADDITIVES FOR CULTURE MEDIA, 4240009
Primary DI / UDI-DI
08056450503273
Basic UDI-DI
805645050SUPPLEMENTS042E9
EMDN Code
W0104010104 Additives for dcm (growth supplements, selective agents, ...)
Device Class
Class A
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000018174

Other devices from Biolife Italiana s.r.l.

See all devices from Biolife Italiana s.r.l. →

Properties

  • Professional Testing

Other properties (10)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No