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Rocket Post VAT's Insertion Set

by Rocket Medical Plc

Ref R54400-16-MI

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 7 Nov 2026. What this means

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number50552709PP13AEZ Basic UDI-DI 05055270976819UDI-DIDate27 Oct 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  • Withdrawn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
TF_R013 PP IPC IIb
Model / Reference
R54400-16-MI
Primary DI / UDI-DI
05055270976819
Basic UDI-DI
50552709PP13AEZ
EMDN Code
A060299 Percutaneous drainage systems - other
Device Class
Class IIb
Medical Purpose
The procedure pack is intended to combine devices which have their own individual intended purposes.

Manufacturer details

EUDAMED SRN
GB-PR-000030677

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Properties

  • Sterile