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ASSI.JFCL318D.2

by Accurate Surgical & Scientific Instruments Corp.

ASSI.JFCL318D.2 is a Class I device made by Accurate Surgical & Scientific Instruments Corp., listed in FDA GUDID since 10 Aug 2023 (UDI-DI 00841645102939), 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 Number00841645102939 UDI-DI Date10 Aug 2023ListedStatusListed 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  • Withdrawn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
Vascular dilator, reusable
Model / reference
ASSI.JFCL318D.2
Description
Vessel Dilator 18cm Flt Hdl. 9mm wide, Curved 0.2mm tip dia.
Primary DI / UDI-DI
00841645102939
FDA product code
HNR
GMDN term
Vascular dilator, reusable
Device class
Class I
Regulation number
886.4350
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Vascular dilator, reusable

Other devices from Accurate Surgical & Scientific Instruments Corp.

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Properties

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