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Orthopaedic Packs

by Ivor Shaw Limited 40 variants

Ref CTP-35000 Rev.2

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5033241PACKORTHO3R Basic UDI-DI 05033241068275UDI-DIDate27 Sep 2022RegisteredStatusActive

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  • Withdrawn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
Orthopaedic Packs
Model / Reference
CTP-35000 Rev.2
Primary DI / UDI-DI
05033241068275
Basic UDI-DI
5033241PACKORTHO3R
EMDN Code
V0501 Clinical emergency kits
Device Class
Class IIb
Medical Purpose
Packs intended for Orthopaedic procedures

Manufacturer details

EUDAMED SRN
GB-PR-000023775

Other devices from Ivor Shaw Limited

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Properties

  • Sterile