MTAPUID1832CLRD
by Qfix
Part of a family of 188 devices: see the family page
Ref MTAPUID1832CLRDModel Aquaplast RT and Fibreplast
MTAPUID1832CLRD 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
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number8419621RTTHERMOPF 00841439110218 | Date22 May 2026 | StatusActive |
Official records
- EUDAMED public site 8419621RTTHERMOPF
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Model / reference
- Aquaplast RT and Fibreplast, MTAPUID1832CLRD
- Primary DI / UDI-DI
- 00841439110218
- 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
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