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Presto Första Hjälpen väska M - Komplett

by Presto AB

Ref 114362

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 Number732301BFAMPZU Basic UDI-DI 07323011143621UDI-DIDate15 Apr 2026RegisteredStatusActive

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  • Withdrawn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

Device Name
Presto Första Hjälpen väska M - Komplett
Model / Reference
114362
Primary DI / UDI-DI
07323011143621
Basic UDI-DI
732301BFAMPZU
EMDN Code
M9099 General and specialist medical devices – other (suture patches see h900102)
Device Class
Class IIa
Medical Purpose
Första hjälpenprodukter för behandling av skador och sår

Manufacturer details

EUDAMED SRN
SE-PR-000052372

Other devices from Presto AB

See all devices from Presto AB →

Properties

Other properties (1)

  • Sterile: No