Aquatyphoon
Ref AQUATYPHOON
Aquatyphoon is a Class I device made by Plasmabiotics, registered in EUDAMED on 21 Aug 2026 (Basic UDI-DI 37013544A03-000CA), 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 | Number37013544A03-000CA | Date21 Aug 2026 | StatusActive |
Official records
- EUDAMED public site 37013544A03-000CA
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- Withdrawn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
- AQUATYPHOON
- Primary DI / UDI-DI
- 03701354420113, 03701354420144, 03701354420120, 03701354420137, 03701354420151, 03701354420106
- Basic UDI-DI
- 37013544A03-000CA
- EMDN code
- Z12011311 Endoscope washers
- Device class
- Class I
- EU registration type
- Standard device
- EU market of registration
- France
Manufacturer details
- EUDAMED SRN
- FR-MF-000003777
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