Skip to content

Hyggilam Plus bäddset Lakan örngott spärrskikt

by Cellcomb AB

Ref 800005

Active European Union

CE MDR

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number732189Set5F Basic UDI-DI 17321890000094UDI-DIDate16 Jun 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Disposable Non-Sterile Procedure Pack
Model / Reference
800005
Primary DI / UDI-DI
17321890000094
Basic UDI-DI
732189Set5F
EMDN Code
T0299 Protection drapes and garments - other
Device Class
Class I
Medical Purpose
For use as a non-sterile disposable procedure pack to support patient preparation, bedding, draping and general medical care procedures

Manufacturer details

EUDAMED SRN
SE-PR-000053613

Other devices from Cellcomb

See all devices from Cellcomb →

Properties

Other properties (1)

  • Sterile: No