Iu 8175-06
Ref IU 8175-06Model Instrument
Iu 8175-06 is a Class I device made by aap Implantate AG, registered in EUDAMED on 3 Jun 2026 (Basic UDI-DI 40424090081H7) and listed in FDA GUDID since 28 Feb 2018 (UDI-DI 04042409220081), active as of 23 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number40424090081H7 04042409220081 | Date3 Jun 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04042409220081 | Date28 Feb 2018 | StatusListed |
Official records
- EUDAMED public site 40424090081H7
- AccessGUDID record 04042409220081
Across registries
- EUDAMED Basic UDI-DI 40424090081H7 registered 3 Jun 2026 Active
- FDA GUDID UDI-DI 04042409220081 listed 28 Feb 2018 Listed
Timeline
- Listed FDA GUDID 04042409220081
- Registered EUDAMED 40424090081H7
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Orthopaedic implant-instrument extension adaptor, reusable
- Model / reference
- IU 8175-06, Instrument
- Primary DI / UDI-DI
- 04042409220081
- Basic UDI-DI
- 40424090081H7
- FDA product code
- LXH
- EMDN code
- L098099 Orthopaedic and traumatological surgery instruments, reusable - other accessories
- GMDN term
- Orthopaedic implant-instrument extension adaptor, reusable
- Device class
- Class I
- Regulation number
- 888.4540
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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