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MediChoice EP1500

by Owens & Minor Distribution, Inc.

MediChoice EP1500 is a Class I device made by Owens & Minor Distribution, Inc., listed in FDA GUDID since 30 Sep 2020 (UDI-DI 10885632109966), 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 Number10885632109966 UDI-DI Date30 Sep 2020ListedStatusListed 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  • Withdrawn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
MediChoice
Generic name
Eye splash shield, single-use
Model / reference
EP1500
Primary DI / UDI-DI
10885632109966
FDA product code
HOY
GMDN term
Eye splash shield, single-use
Device class
Class I
Regulation number
886.4750
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code HOY (Shield, eye, ophthalmic (including sunlamp protective eyewear and post-mydriatic eyewear)).

Other devices from Owens & Minor Distribution, Inc.

See all devices from Owens & Minor Distribution, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)