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Vitros 6800874

by Ortho-Clinical Diagnostics

Vitros 6800874 is a Class I device made by Ortho-Clinical Diagnostics, listed in FDA GUDID since 8 Apr 2020 (UDI-DI 10758750000951), 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 Number10758750000951 UDI-DI Date8 Apr 2020ListedStatusListed 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  • Withdrawn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
Vitros
Generic name
Total cortisol IVD, kit, chemiluminescent immunoassay
Model / Ref / Catalog
6800874
Primary DI / UDI-DI
10758750000951
FDA product code
JJX
GMDN term
Total cortisol IVD, kit, chemiluminescent immunoassay
Device class
Class I
Regulation number
862.1660
GUDID distribution status
In Commercial Distribution

Related devices

Category: Total cortisol IVD, kit, chemiluminescent immunoassay

Similar devices in this category

Other devices filed under Total cortisol IVD, kit, chemiluminescent immunoassay.

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Properties

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