Iu 7960-00
Ref IU 7960-00Model Instrument
Iu 7960-00 is a Class I device made by aap Implantate AG, registered in EUDAMED on 17 Sep 2026 (Basic UDI-DI B-04042409259449) and listed in FDA GUDID since 28 Feb 2018 (UDI-DI 04042409259449), active as of 23 Oct 2026.
Active
CE MDD
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/MDD EUDAMED | NumberB-04042409259449 04042409259449 | Date17 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04042409259449 | Date28 Feb 2018 | StatusListed |
Official records
- EUDAMED public site B-04042409259449
- AccessGUDID record 04042409259449
Across registries
- EUDAMED Basic UDI-DI B-04042409259449 registered 17 Sep 2026 Active
- FDA GUDID UDI-DI 04042409259449 listed 28 Feb 2018 Listed
Timeline
- Listed FDA GUDID 04042409259449
- Registered EUDAMED B-04042409259449
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Surgical depth gauge, reusable
- Model / reference
- IU 7960-00, Instrument
- Primary DI / UDI-DI
- 04042409259449
- Basic UDI-DI
- B-04042409259449
- FDA product code
- HTJ
- EMDN code
- L0923 Orthopaedics surgical measurers, reusable
- GMDN term
- Surgical depth gauge, reusable
- Device class
- Class I
- Regulation number
- 888.4300
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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