EF1 Dne-1000-Hfb
EF1 Dne-1000-Hfb is a Class II device made by Medshape, Inc., cleared under FDA 510(k) K113106 on 4 Jan 2012 and listed in FDA GUDID since 31 May 2024 (UDI-DI 00810028397132), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00810028397132 | Date31 May 2024 | StatusListed |
| United States | FDA 510(k)SESE | NumberK113106 | Date4 Jan 2012 | StatusActive |
Official records
- AccessGUDID record 00810028397132
- FDA 510(k) database K113106
Across registries
- FDA 510(k) K113106 decided 4 Jan 2012 Active
- FDA GUDID UDI-DI 00810028397132 listed 31 May 2024 Listed
Timeline
- Cleared FDA 510(k) K113106
- Listed FDA GUDID 00810028397132
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- EF1
- Generic name
- External orthopaedic fixation system noninvasive component, single-use
- Model / reference
- DNE-1000-HFB
- Primary DI / UDI-DI
- 00810028397132
- 510(k) Number
- FDA product code
- KTT
- GMDN term
- External orthopaedic fixation system noninvasive component, single-use
- Device class
- Class II
- Regulation number
- 888.3030
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- MRI safety
- MR Unsafe
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