Black Bipolar Jensen Bayonet Forceps 2700-880NS
by Sontec Instruments, Inc. 2 variants
Active
510(k)
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | NumberB0992700880NS0 | Date14 Oct 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK101080 | Date21 Jun 2010 | StatusActive |
Recalls
No FDA recalls found in the data synced 23 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Black Bipolar Jensen Bayonet Forceps
- Generic name
- Endoscopic electrosurgical handpiece/electrode, bipolar, reusable
- Model / reference
- 2700-880NS
- Primary DI / UDI-DI
- B0992700880NS0
- 510(k) Number
- FDA product code
- GEI
- GMDN term
- Endoscopic electrosurgical handpiece/electrode, bipolar, reusable
- Device class
- Class II
- Regulation number
- 878.4400
- GUDID distribution status
- Not in Commercial Distribution
- Size
- Length — 6 Inch
Other devices from Sontec Instruments, Inc.
Properties
Other properties (12)
- Supplied sterile: No
- Single use: No
- Implantable: No
- Contains latex: No
- Over-the-counter: No
- Convenience kit: No
- Combination product: No
- HCT/P: No
- Premarket exempt: No
- Serial number: No
- Expiration date: No
- Manufacturing date: No