BiSurge 628-163-920
by Genicon
BiSurge 628-163-920 is a Class I device made by Genicon, listed in FDA GUDID since 11 Oct 2017 (UDI-DI 00877972006657), 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 | Number00877972006657 | Date11 Oct 2017 | StatusListed |
Official records
- AccessGUDID record 00877972006657
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- BiSurge
- Generic name
- Laparoscopic access cannula, single-use
- Model / reference
- 628-163-920
- Primary DI / UDI-DI
- 00877972006657
- FDA product code
- GEA, GEI
- GMDN term
- Laparoscopic access cannula, single-use
- Device class
- Class I
- Regulation number
- 878.4800, 878.4400
- GUDID distribution status
- In Commercial Distribution
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