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WMA-Strip

by W.H.P.M. Inc.

WMA-Strip is a Class II device made by W.H.P.M. Inc., listed in FDA GUDID since 1 Aug 2016 (UDI-DI 00841824101760), 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 Number00841824101760 UDI-DI Date1 Aug 2016ListedStatusListed 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  • Withdrawn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

Generic name
Methamphetamine-specific IVD, kit, rapid ICT, clinical
Model / Ref / Catalog
WMA-Strip
Description
DOA Single Test Strip, 100Pcs/Box Clia Waived mAMP
Primary DI / UDI-DI
00841824101760
FDA product code
LAF
GMDN term
Methamphetamine-specific IVD, kit, rapid ICT, clinical
Device class
Class II
Regulation number
862.3610
GUDID distribution status
In Commercial Distribution

Related devices

Category: Methamphetamine-specific IVD, kit, rapid ICT, clinical

Other devices from W.H.P.M. Inc.

See all devices from W.H.P.M. Inc. →

Properties

  • Single use
  • Prescription use
  • Over-the-counter
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)