TEG5000 07-045
TEG5000 07-045 is a Class II device made by Haemonetics Corporation, cleared under FDA 510(k) K993678 on 5 May 2000 and listed in FDA GUDID since 30 May 2017 (UDI-DI 10812747018210), 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 | Number10812747018210 | Date30 May 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK993678 | Date5 May 2000 | StatusActive |
Official records
- AccessGUDID record 10812747018210
- FDA 510(k) database K993678
Across registries
- FDA 510(k) K993678 decided 5 May 2000 Active
- FDA GUDID UDI-DI 10812747018210 listed 30 May 2017 Listed
Timeline
- Cleared FDA 510(k) K993678
- Listed FDA GUDID 10812747018210
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- TEG5000
- Generic name
- Multiple coagulation marker IVD, control
- Model / reference
- 07-045
- Primary DI / UDI-DI
- 10812747018210
- 510(k) Number
- FDA product code
- JPA
- GMDN term
- Multiple coagulation marker IVD, control
- Device class
- Class II
- Regulation number
- 864.5425
- GUDID distribution status
- In Commercial Distribution
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