P23303-75
by Foosin Medical Supplies Inc., Ltd.
Ref P23303-75Model Polypropylene
P23303-75 is a Class III device made by Foosin Medical Supplies Inc., Ltd., registered in EUDAMED on 17 Sep 2026 (Basic UDI-DI B-06941813680802), active as of 7 Nov 2026.
Active
CE MDD
Valid until
No date given
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD | NumberB-06941813680802 | Date17 Sep 2026 | StatusActive |
Official records
- EUDAMED public site B-06941813680802
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDD Active
EU market availability
Made available in 12 countries, as listed in EUDAMED:
- Belgium since 12 Jun 2026
- Bulgaria since 12 Jun 2026
- Denmark since 12 Jun 2026
- France since 12 Jun 2026
- Germany since 12 Jun 2026
- Greece since 12 Jun 2026
- Hungary since 12 Jun 2026
- Italy since 12 Jun 2026
- Lithuania since 12 Jun 2026
- Poland since 12 Jun 2026
- Romania since 12 Jun 2026
- Spain since 12 Jun 2026
Specification
- Model / reference
- Polypropylene, P23303-75
- Primary DI / UDI-DI
- 06941813680802, 06941813680857, 06941813654629
- Basic UDI-DI
- B-06941813680802, B-06941813680857, B-06941813654629
- Direct marketing DI
- 06941813654629
- EMDN code
- H010201010401, H010201010402
- Device class
- Class III
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- LithuaniaGreece
Manufacturer details
- EUDAMED SRN
- CN-MF-000006957
- Authorised representative
- MedNet EC-REP GmbH DE-AR-000000002
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