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Ezy Dose 70281

by Apothecary Products, Inc.

Ezy Dose 70281 is a Class I device made by Apothecary Products, Inc., listed in FDA GUDID since 5 Nov 2020 (UDI-DI 00025715012179), 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 Number00025715012179 UDI-DI Date5 Nov 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  • Withdrawn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
Ezy Dose
Generic name
Pill crusher/splitter
Model / reference
70281
Primary DI / UDI-DI
00025715012179
FDA product code
OHY
GMDN term
Pill crusher/splitter
Device class
Class I
Regulation number
880.6430
GUDID distribution status
In Commercial Distribution

Related devices

Category: Pill crusher/splitter

Other devices from Apothecary Products, Inc.

See all devices from Apothecary Products, Inc. →

Properties

  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)