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Trupack® Qan

by Trusetal Verbandstoffwerk GmbH

Ref DEKA129-01S

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 Number4026267TRPA001SN Basic UDI-DI 04026267005219UDI-DIDate20 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  • Withdrawn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
Trupack®
Model / Reference
DEKA129-01S
Primary DI / UDI-DI
04026267005219
Basic UDI-DI
4026267TRPA001SN
EMDN Code
Q0299 Ophthalmic devices - other
Device Class
Class IIa
Medical Purpose
Customised procedure pack, particularly for ophthalmology.

Manufacturer details

EUDAMED SRN
DE-PR-000028751

Properties

  • Sterile