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Bipolar Jensen Bayonet Forceps 2700-890

by Sontec Instruments, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00192896010758 UDI-DI Date24 Aug 2018ListedStatusListed GUDID: 1 of 2 UDI-DIs in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Bipolar Jensen Bayonet Forceps
Generic Name
Endoscopic electrosurgical handpiece/electrode, bipolar, reusable
Model / Reference
2700-890
Primary DI / UDI-DI
00192896010758, B09927008900
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
In Commercial Distribution (UDI-DI 00192896010758)
Not in Commercial Distribution (UDI-DI B09927008900)
Size
Length — 7 Inch

Related devices

Category: Endoscopic electrosurgical handpiece/electrode, bipolar, reusable

Cleared under the same submission (K101080)

Show all (12)

Other devices from Sontec Instruments, Inc.

See all devices from Sontec Instruments, Inc. →

Properties

  • Prescription Use
  • Lot / Batch Number

Other properties (12)

  • 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