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Chorus Trio 81200

by Diesse Diagnostica Senese SpA

Chorus Trio 81200 is a Class I device made by Diesse Diagnostica Senese SpA, listed in FDA GUDID since 14 Dec 2023 (UDI-DI 08033891328856), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08033891328856 UDI-DI Date14 Dec 2023ListedStatusListed 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  • Withdrawn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
Chorus Trio
Generic name
Enzyme immunoassay (EIA) analyser IVD
Model / Ref / Catalog
81200
Primary DI / UDI-DI
08033891328856
FDA product code
JJE
GMDN term
Enzyme immunoassay (EIA) analyser IVD
Device class
Class I
Regulation number
862.2160
GUDID distribution status
In Commercial Distribution

Related devices

Category: Enzyme immunoassay (EIA) analyser IVD

Similar devices in this category

Other devices filed under Enzyme immunoassay (EIA) analyser IVD.

Other devices from Diesse Diagnostica Senese SpA

See all devices from Diesse Diagnostica Senese SpA →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)