Skip to content

Arvolife Drug Test Panel

by Clinical Guard

Arvolife Drug Test Panel is a Class II device made by Clinical Guard, listed in FDA GUDID since 27 Mar 2018 (UDI-DI 00851950008147), 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 Number00851950008147 UDI-DI Date27 Mar 2018ListedStatusListed 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  • Withdrawn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
Arvolife
Generic name
Multiple drugs of abuse IVD, kit, rapid ICT, clinical
Model / reference
Drug Test Panel
Primary DI / UDI-DI
00851950008147
FDA product code
JXM, DKZ, LDJ, DIO, DJG
GMDN term
Multiple drugs of abuse IVD, kit, rapid ICT, clinical
Device class
Class II
Regulation number
862.3170, 862.3100, 862.3870, 862.3250, 862.3650
GUDID distribution status
In Commercial Distribution

Related devices

Category: Multiple drugs of abuse IVD, kit, rapid ICT, clinical

Similar devices in this category

Other devices filed under Multiple drugs of abuse IVD, kit, rapid ICT, clinical.

Other devices from Clinical Guard

See all devices from Clinical Guard →

Properties

  • Single use
  • Over-the-counter
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)