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Pack Epidural

by Unisurge International Ltd 2 variants

Ref F100012

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5053488F1QM Basic UDI-DI 05053488002450UDI-DIDate23 Mar 2023RegisteredStatusActive

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  • Withdrawn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
F1 Product Family - Procedure Packs Used For Anaesthetic Procedures
Model / Reference
F100012
Primary DI / UDI-DI
05053488002450
Basic UDI-DI
5053488F1QM
EMDN Code
A01030102 Epidural anaesthesia needles and kits
Device Class
Class I
Medical Purpose
Procedure Pack

Manufacturer details

EUDAMED SRN
GB-PR-000033353

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Properties

  • Sterile