UdiWatchPublic device page
Patient kit XL
Record
- UDI-DI
- 07611600996797
- Basic UDI-DI
- 76116003703MV
- Status
- Not intended for the EU market
- Risk class
- Class I
- Reference
- 990539
- Version
- 1
- Manufacturer
- IVF HARTMANN AG
- Manufacturer SRN
- CH-PR-000019926
- Manufacturer status
- Active
Last read from the public register: 2026-11-01T19:21:38+00:00.
UdiWatch is independent and not affiliated with the European Commission. This page shows our last read of the public EUDAMED register. If it differs from EUDAMED, EUDAMED is right.