Thd Biopsy (J)
by Thd SpA
Thd Biopsy (J) (800317) is a Class I device made by Thd SpA, listed in FDA GUDID since 20 Feb 2025 (UDI-DI 08051887045754), 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 | Number08051887045754 | Date20 Feb 2025 | StatusListed |
Official records
- AccessGUDID record 08051887045754
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Thd Biopsy
- Generic name
- Rigid endoscopic biopsy forceps, single-use
- Model / Ref / Catalog
- THD BIOPSY (J), 800317
- Primary DI / UDI-DI
- 08051887045754
- FDA product code
- FCL
- GMDN term
- Rigid endoscopic biopsy forceps, single-use
- Device class
- Class I
- Regulation number
- 876.1075
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 18 Centimeter
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