Assupro
by Assut Europe SpA 441 variants
Part of a family of 446 devices: see the family page
Ref PX900
Assupro (PX900) is a Class III device made by Assut Europe SpA, registered in EUDAMED on 6 Mar 2026 (Basic UDI-DI 8033439ASSUPRO4P) with CE/MDR certificate CVD0048250326 valid until 7 Aug 2028, active as of 24 Oct 2026.
Active
CE MDR
Valid until
7 Aug 2028
FDA recalls
Not applicable
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number8033439ASSUPRO4P 38033439438314 | Date6 Mar 2026 | StatusActive |
Official records
- EUDAMED public site 8033439ASSUPRO4P
Certificates
- CVD0048250326 Active
Technical documentation EU MDR
- Certifier
- ISTITUTO SUPERIORE DI SANITA' 0373
- Issued
- 28 Jan 2026
- Expires
- 7 Aug 2028
- Reason
- Change approved
Timeline
- Certificate issued EUDAMED CVD0048250326
- Registered EUDAMED 8033439ASSUPRO4P
- Certificate expires EUDAMED CVD0048250326
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Model / reference
- PX900
- Primary DI / UDI-DI
- 38033439438314
- Basic UDI-DI
- 8033439ASSUPRO4P
- Direct marketing DI
- 38033439438314
- EMDN code
- H010201010402 Polypropylene monofilament with needle for video surgery
- Device class
- Class III
- EU registration type
- Standard device
- EU market of registration
- Italy
Manufacturer details
- EUDAMED SRN
- IT-MF-000018178
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