diagnostic FTRD Set 13
diagnostic FTRD Set 13 (200.76) is a Class II device made by Ovesco Endoscopy AG, listed in FDA GUDID since 2 Oct 2018 (UDI-DI 04260206311072), 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 | Number04260206311072 | Date2 Oct 2018 | StatusListed |
Official records
- AccessGUDID record 04260206311072
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- diagnostic FTRD Set
- Generic name
- Endoscopic electrosurgical full-thickness tissue biopsy/resection set
- Model / Ref / Catalog
- 13, 200.76
- Primary DI / UDI-DI
- 04260206311072
- FDA product code
- OCZ, KNS, FDI, PKL
- GMDN term
- Endoscopic electrosurgical full-thickness tissue biopsy/resection set
- Device class
- Class II
- Regulation number
- 876.1500, 876.4300, 876.4400
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional
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