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MedTest DX Control Level 1 HNC200

by Medtest DX

MedTest DX Control Level 1 HNC200 is a Class I device made by Medtest DX, listed in FDA GUDID since 30 Sep 2016 (UDI-DI 00817439020901), not in commercial distribution (GUDID) as of 22 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 Number00817439020901 UDI-DI Date30 Sep 2016ListedStatusListed GUDID: not 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  • Withdrawn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
MedTest DX Control Level 1
Generic name
Multiple-type clinical chemistry analyte profile IVD, control
Model / Ref / Catalog
HNC200
Primary DI / UDI-DI
00817439020901
FDA product code
JJY
GMDN term
Multiple-type clinical chemistry analyte profile IVD, control
Device class
Class I
Regulation number
862.1660
GUDID distribution status
Not in Commercial Distribution

Similar devices

Other devices filed under FDA product code JJY (Multi-Analyte Controls, All Kinds (Assayed)).

Other devices from Medtest DX

See all devices from Medtest DX →

Properties

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