00710802
by US Endoscopy
00710802 is a Class II device made by US Endoscopy, listed in FDA GUDID since 17 Sep 2016 (UDI-DI 00816765010761), not in commercial distribution (GUDID) as of 22 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 | Number00816765010761 | Date17 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00816765010761
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Enteral feeding kit, adult/paediatric, sterile
- Model / Ref / Catalog
- 00710802
- Primary DI / UDI-DI
- 00816765010761
- FDA product code
- KNT
- GMDN term
- Enteral feeding kit, adult/paediatric, sterile
- Device class
- Class II
- Regulation number
- 876.5980
- GUDID distribution status
- Not in Commercial Distribution
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