Endoch EAI-0684
by Endoch Inc
Endoch EAI-0684 is a Class I device made by Endoch Inc, listed in FDA GUDID since 1 Jun 2019 (UDI-DI EAI0684), 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 | NumberEAI0684 | Date1 Jun 2019 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Endoch
- Generic name
- Rigid endoscopic grasping forceps, single-use
- Model / Ref / Catalog
- EAI-0684
- Primary DI / UDI-DI
- EAI0684
- FDA product code
- GEN, GEI
- GMDN term
- Rigid endoscopic grasping forceps, single-use
- Device class
- Class I
- Regulation number
- 878.4800, 878.4400
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code GEN (Forceps, General & Plastic Surgery).
- SCANLAN® Forceps 4004-235 by SCANLAN INTERNATIONAL INC
- CUP BIOPSY FORCEP, 1.7MM by Arthropedics, Inc.
- SCANLAN® Miscellaneous Instruments 4004-15 by SCANLAN INTERNATIONAL INC
- Gimmi CB.1387.16 by Gimmi GmbH
- MicroFrance® M832 by Integra Microfrance
- MicroFrance® M801 by Integra Microfrance
- Surtex GY-581-24 by SURTEX INSTRUMENTS LTD.
- GRASPING FORCEP, 1.7MM by Arthropedics, Inc.
- Gimmi CB.1391.20 by Gimmi GmbH
- Surtex GY-550-25 by SURTEX INSTRUMENTS LTD.