Daniels 1003107505
by Daniels Corporation International Pty Ltd
Daniels 1003107505 is a Class II device made by Daniels Corporation International Pty Ltd, cleared under FDA 510(k) K001337 on 5 Jul 2000 and listed in FDA GUDID since 7 Mar 2019 (UDI-DI 09333990004422), active as of 23 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 | Number09333990004422 | Date7 Mar 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK001337 | Date5 Jul 2000 | StatusActive |
Official records
- AccessGUDID record 09333990004422
- FDA 510(k) database K001337
Across registries
- FDA 510(k) K001337 decided 5 Jul 2000 Active
- FDA GUDID UDI-DI 09333990004422 listed 7 Mar 2019 Listed
Timeline
- Cleared FDA 510(k) K001337
- Listed FDA GUDID 09333990004422
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Daniels
- Generic name
- Sharps container
- Model / reference
- 1003107505
- Primary DI / UDI-DI
- 09333990004422
- 510(k) Number
- FDA product code
- MMK
- GMDN term
- Sharps container
- Device class
- Class II
- Regulation number
- 880.5570
- GUDID distribution status
- In Commercial Distribution
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