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Amplim A8171-3-Dv

by Amplim, LLC

Amplim A8171-3-Dv is a Class II device made by Amplim, LLC, listed in FDA GUDID since 5 Jun 2024 (UDI-DI 00810477026201), 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 Number00810477026201 UDI-DI Date5 Jun 2024ListedStatusListed 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  • Withdrawn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
Amplim
Generic name
Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical
Model / reference
A8171-3-DV
Primary DI / UDI-DI
00810477026201
FDA product code
LCX
GMDN term
Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical
Device class
Class II
Regulation number
862.1155
GUDID distribution status
In Commercial Distribution

Related devices

Category: Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical

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Other devices filed under Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical.

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Properties

  • Single use
  • Lot / batch number
  • Expiration date
Other properties (12, all answered No)