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Rapid Diagnostics M-Amphamphetamine Test Strip 07RD7005

by Rapid Diagnostics Inc

Rapid Diagnostics M-Amphamphetamine Test Strip 07RD7005 is a Class II device made by Rapid Diagnostics Inc, listed in FDA GUDID since 20 Oct 2016 (UDI-DI 00817830020029), 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 Number00817830020029 UDI-DI Date20 Oct 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  • Withdrawn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

Trade name
Rapid Diagnostics M-Amphamphetamine Test Strip
Generic name
Methamphetamine-specific IVD, kit, rapid ICT, clinical
Model / Ref / Catalog
07RD7005
Primary DI / UDI-DI
00817830020029
FDA product code
DJC
GMDN term
Methamphetamine-specific IVD, kit, rapid ICT, clinical
Device class
Class II
Regulation number
862.3610
GUDID distribution status
In Commercial Distribution
Size
Length — 72 Millimeter

Related devices

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

Other devices from Rapid Diagnostics Inc

See all devices from Rapid Diagnostics Inc →

Properties

  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)