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Procedure Pack

by Fapomed- Dispositivos Médicos, S.A. 4 variants

Ref 407-2026/1

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number56009615PP2017745221BR Basic UDI-DI 05600961550511UDI-DIDate29 May 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  • Withdrawn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
Procedure Pack
Model / Reference
407-2026/1
Primary DI / UDI-DI
05600961550511
Basic UDI-DI
56009615PP2017745221BR
EMDN Code
V0599 Clinical procedures kits not included in other classes - other
Device Class
Class I
Medical Purpose
Systems and Procedure Packs are combinations of products packaged together and placed on the market with the intention of being used for a specific medical purpose.

Manufacturer details

EUDAMED SRN
PT-PR-000004889

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Properties

Other properties (1)

  • Sterile: No