TDNexLabs
by Technidata
TDNexLabs is a Class I device made by Technidata, listed in FDA GUDID since 8 Aug 2022 (UDI-DI 03770027519003), registry data as of 31 May 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number03770027519003 | Date8 Aug 2022 | StatusListed |
Official records
- AccessGUDID record 03770027519003
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Clinical laboratory information system application software
- Model / reference
- TDNexLabs
- Primary DI / UDI-DI
- 03770027519003
- FDA product code
- JQP
- GMDN term
- Clinical laboratory information system application software
- Device class
- Class I
- Regulation number
- 862.2100
- GUDID distribution status
- In Commercial Distribution
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