Targon Ph/H KH188R
by Aesculap AG
Ref KH188R
Targon Ph/H KH188R is a device classified as Class IIa in the EU and Class I in the US made by Aesculap AG, registered in EUDAMED on 16 Oct 2026 (Basic UDI-DI B-04038653262595) and listed in FDA GUDID since 20 May 2020 (UDI-DI 04038653262595), active as of 12 Nov 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-04038653262595 04038653262595 | Date16 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04038653262595 | Date20 May 2020 | StatusListed |
Official records
- EUDAMED public site B-04038653262595
- AccessGUDID record 04038653262595
Across registries
- EUDAMED Basic UDI-DI B-04038653262595 registered 16 Oct 2026 Active
- FDA GUDID UDI-DI 04038653262595 listed 20 May 2020 Listed
Timeline
- Listed FDA GUDID 04038653262595
- Registered EUDAMED B-04038653262595
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Targon Ph/H
- Generic name
- Orthopaedic prosthesis implantation positioning instrument, reusable
- Model / Ref / Catalog
- KH188R
- Primary DI / UDI-DI
- 04038653262595
- Basic UDI-DI
- B-04038653262595
- FDA product code
- LXH
- EMDN code
- L091199 Orthopaedic prosthetics instruments, reusable - other
- GMDN term
- Orthopaedic prosthesis implantation positioning instrument, reusable
- Device class
- Class IIa EUDAMEDClass I GUDID
- Regulation number
- 888.4540
- 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
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class IIa | Class I |
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