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ASSI.FOAHL280

by Accurate Surgical & Scientific Instruments Corp.

ASSI.FOAHL280 is a Class II device made by Accurate Surgical & Scientific Instruments Corp., listed in FDA GUDID since 26 Sep 2016 (UDI-DI 00841645131861), registry data as of 22 Oct 2026.

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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00841645131861 UDI-DI Date26 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Assi
Generic name
Fibreoptic light cable, reusable
Model / reference
ASSI.FOAHL280
Description
Adapter for Fiber Optic Headlight Storz Type
Primary DI / UDI-DI
00841645131861
FDA product code
FCW
GMDN term
Fibreoptic light cable, reusable
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

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Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)