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MTAPUID1824

by Qfix

Ref MTAPUID1824Model Aquaplast RT and Fibreplast

MTAPUID1824 is a Class I device made by Qfix, registered in EUDAMED on 22 May 2026 (Basic UDI-DI 8419621RTTHERMOPF), active as of 7 Nov 2026.

Active European Union

CE MDR

Valid until

No date given

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

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8419621RTTHERMOPF Basic UDI-DI 00841439103647UDI-DIDate22 May 2026RegisteredStatusActive

Official records

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  • Withdrawn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

Model / reference
Aquaplast RT and Fibreplast, MTAPUID1824
Primary DI / UDI-DI
00841439103647
Basic UDI-DI
8419621RTTHERMOPF
EMDN code
Z12011299 Patient positioning instruments – other
Device class
Class I
EU registration type
Standard device
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
US-MF-000002762
Authorised representative
Advena SRL IT-AR-000051131

Similar devices in this category

Other devices filed under PATIENT POSITIONING INSTRUMENTS – OTHER.

Other devices from Qfix

See all devices from Qfix →

Properties

Other properties (14, all answered No)