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Pocguide Multi-Drug Test Cup 1

by Hangzhou Aichek Medical Technology Co., Ltd. 4 variants

Active European Union. Also listed in GUDID (US).

CE IVDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing GUDID Number06978151200027 UDI-DI Date24 Dec 2024ListedStatusListed GUDID: in commercial distribution
European UnionCE/IVDD EUDAMED Number— Date—StatusActive

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/IVDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Pocguide Multi-Drug Test Cup
Generic Name
Multiple drugs of abuse IVD, kit, rapid ICT, clinical
Model / Reference
1
Primary DI / UDI-DI
06978151200027
FDA Product Code
NFT, NGL, PTH, NFV, NFY, PTG, NGG, NGM, QAW, NFW
GMDN Term
Multiple drugs of abuse IVD, kit, rapid ICT, clinical
Device Class
Class II
Regulation Number
862.3100, 862.3650, 862.3150, 862.3170, 862.3250, 862.3620, 862.3610, 862.3910, 862.3870
GUDID distribution status
In Commercial Distribution

Other devices from Hangzhou Aichek Medical Technology Co., Ltd.

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Properties

  • Single Use
  • Over-the-Counter
  • Convenience Kit
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No