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Omni® Hysteroscopic Grasper OMNI-G-DSI-001

by Suzhou AcuVu medical technology Co., Ltd.

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06974880994343 UDI-DI Date17 Apr 2026ListedStatusListed 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  • Withdrawn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
Omni® Hysteroscopic Grasper
Generic Name
Rigid endoscopic scissors, single-use
Model / Reference
OMNI-G-DSI-001
Primary DI / UDI-DI
06974880994343
FDA Product Code
NWW
GMDN Term
Rigid endoscopic scissors, single-use
Device Class
Class I
Regulation Number
884.1690
GUDID distribution status
In Commercial Distribution

Other devices from Suzhou AcuVu medical technology Co., Ltd.

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No