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Bipolar Iris Forceps 2700-935

by Sontec Instruments, Inc. 2 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

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 Number00192896006492 UDI-DI Date22 Aug 2018ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Bipolar Iris Forceps
Generic Name
Endoscopic electrosurgical handpiece/electrode, bipolar, reusable
Model / Reference
2700-935
Primary DI / UDI-DI
00192896006492
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
Size
Length — 3.25 Inch

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