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MediBrief MB17002

by Medi-Tech International Corporation

MediBrief MB17002 is a Class I device made by Medi-Tech International Corporation, listed in FDA GUDID since 1 Jul 2019 (UDI-DI 00027479211720), 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 Number00027479211720 UDI-DI Date1 Jul 2019ListedStatusListed 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  • Withdrawn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
MediBrief
Generic name
Incontinence pants, single-use
Model / Ref / Catalog
MB17002
Primary DI / UDI-DI
00027479211720
FDA product code
EYQ
GMDN term
Incontinence pants, single-use
Device class
Class I
Regulation number
876.5920
GUDID distribution status
In Commercial Distribution

Related devices

Category: Incontinence pants, single-use

Similar devices

Other devices filed under FDA product code EYQ (Garment, Protective, For Incontinence).

Other devices from Medi-Tech International Corporation

See all devices from Medi-Tech International Corporation →

Properties

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