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Meijer 4080389

by Meijer, Inc.

Meijer 4080389 is a Class II device made by Meijer, Inc., listed in FDA GUDID since 31 Mar 2017 (UDI-DI 00713733086141), 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 Number00713733086141 UDI-DI Date31 Mar 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  • Withdrawn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
Meijer
Generic name
Wart-removal cryogenic kit
Model / Ref / Catalog
4080389
Primary DI / UDI-DI
00713733086141
FDA product code
GEH
GMDN term
Wart-removal cryogenic kit
Device class
Class II
Regulation number
878.4350
GUDID distribution status
In Commercial Distribution
Size
Height — 155 Millimeter

Related devices

Category: Wart-removal cryogenic kit

Similar devices

Other devices filed under FDA product code GEH (Unit, Cryosurgical, Accessories).

Other devices from Meijer, Inc.

See all devices from Meijer, Inc. →

Properties

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