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iPRO FHCEP3

by Fannin (UK) Limited

iPRO FHCEP3 is a Class I device made by Fannin (UK) Limited, listed in FDA GUDID since 23 Feb 2023 (UDI-DI 05060654200114), 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 Number05060654200114 UDI-DI Date23 Feb 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  • Withdrawn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
iPRO
Generic name
Eye patch, single-use
Model / reference
FHCEP3
Primary DI / UDI-DI
05060654200114
FDA product code
KGX
GMDN term
Eye patch, single-use
Device class
Class I
Regulation number
880.5240
GUDID distribution status
In Commercial Distribution

Related devices

Category: Eye patch

Similar devices in this category

Other devices filed under Eye patch.

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (10, all answered No)