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Haemo Pack

by Swedish Orphan Biovitrum AB

Ref 07350031444384

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number73500314475000294 Basic UDI-DI 07350031444384UDI-DIDate5 Jun 2024RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
07350031444384
Primary DI / UDI-DI
07350031444384
Basic UDI-DI
73500314475000294
EMDN Code
M0299, M0599, V9099
Device Class
Class I
Medical Purpose
A combination of products to clean the skin, absorb blood to protect minor wounds associated with the self-administration of an infusion medicine in a lay-person (home) setting

Manufacturer details

EUDAMED SRN
SE-PR-000042225

Properties

  • Sterile