Ercp GI112
by Heraeus Medical Components LLC
Ercp GI112 is a Class II device made by Heraeus Medical Components LLC, listed in FDA GUDID since 21 Sep 2016 (UDI-DI 00857834006186), registry data 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 | Number00857834006186 | Date21 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00857834006186
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Ercp
- Generic name
- Gastro-urological guidewire, single-use
- Model / reference
- GI112
- Primary DI / UDI-DI
- 00857834006186
- FDA product code
- OCY
- GMDN term
- Gastro-urological guidewire, single-use
- Device class
- Class II
- Regulation number
- 876.1500
- GUDID distribution status
- In Commercial Distribution
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