Skip to content

Sure-Vue 23048002

by Fisher Scientific Company L.L.C.

Sure-Vue 23048002 is a Class II device made by Fisher Scientific Company L.L.C., listed in FDA GUDID since 12 May 2017 (UDI-DI 10613647001421), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10613647001421 UDI-DI Date12 May 2017ListedStatusListed 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  • Withdrawn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
Sure-Vue
Generic name
Faecal occult blood IVD, kit, rapid ICT, clinical
Model / Ref / Catalog
23048002
Primary DI / UDI-DI
10613647001421
FDA product code
KHE
GMDN term
Faecal occult blood IVD, kit, rapid ICT, clinical
Device class
Class II
Regulation number
864.6550
GUDID distribution status
In Commercial Distribution

Related devices

Category: Faecal occult blood IVD, kit, rapid ICT, clinical

Similar devices

Other devices filed under FDA product code KHE (REAGENT, OCCULT BLOOD).

Other devices from Fisher Scientific Company L.L.C.

See all devices from Fisher Scientific Company L.L.C. →

Properties

  • Single use
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)