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Vitros 6800120

by Ortho-Clinical Diagnostics

Vitros 6800120 is a Class II device made by Ortho-Clinical Diagnostics, listed in FDA GUDID since 10 Aug 2016 (UDI-DI 10758750000593), 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 Number10758750000593 UDI-DI Date10 Aug 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  • Withdrawn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
Vitros
Generic name
Total protein IVD, reagent
Model / Ref / Catalog
6800120
Primary DI / UDI-DI
10758750000593
FDA product code
JGP
GMDN term
Total protein IVD, reagent
Device class
Class II
Regulation number
862.1635
GUDID distribution status
In Commercial Distribution

Related devices

Category: Total protein IVD, reagent

Similar devices in this category

Other devices filed under Total protein IVD, reagent.

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Properties

  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)