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Diamedix MAGO 4S

by Diamedix Corp.

Diamedix MAGO 4S is a Class I device made by Diamedix Corp., listed in FDA GUDID since 21 Sep 2016 (UDI-DI 00817273020471), 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 Number00817273020471 UDI-DI Date21 Sep 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  • Withdrawn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
Diamedix
Generic name
Multichannel clinical chemistry analyser IVD, point-of-care, line-powered
Model / reference
MAGO 4S
Primary DI / UDI-DI
00817273020471
FDA product code
JJF
GMDN term
Multichannel clinical chemistry analyser IVD, point-of-care, line-powered
Device class
Class I
Regulation number
862.2170
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code JJF (Analyzer, Chemistry, Micro, For Clinical Use).

Other devices from Diamedix Corp.

See all devices from Diamedix Corp. →

Properties

  • Lot / batch number
Other properties (14, all answered No)