Depuy 2442-00-000
Depuy 2442-00-000 (244200000) is a Class I device made by Depuy Orthopaedics, Inc., listed in FDA GUDID since 24 Sep 2018 (UDI-DI 10603295124580), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10603295124580 | Date24 Sep 2018 | StatusListed |
Official records
- AccessGUDID record 10603295124580
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Depuy
- Generic name
- Manual goniometer
- Model / Ref / Catalog
- 2442-00-000, 244200000
- Primary DI / UDI-DI
- 10603295124580
- FDA product code
- KQW
- GMDN term
- Manual goniometer
- Device class
- Class I
- Regulation number
- 888.1520
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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