← Back to catalogue

Vitros

FDA UDI

Class II (US FDA UDI)

by Ortho-Clinical Diagnostics

Identity

Trade Name
VITROS FDA UDI
Generic Name
SARS-CoV-2 total antibody IVD, calibrator FDA UDI
Device Name
VITROS Immunodiagnostic Products Anti-SARS-COV-2 Total Calibrator FDA UDI
Model / Reference
6199954 FDA UDI
Description
VITROS Immunodiagnostic Products Anti-SARS-COV-2 Total Calibrator FDA UDI

Identifiers

Catalog Number
6199954 FDA UDI
Primary DI / UDI-DI
10758750033638 FDA UDI
510(k) Number
FDA Product Code
QVP FDA UDI
GMDN Term
SARS-CoV-2 total antibody IVD, calibrator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.3983 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: SARS-CoV-2 total antibody IVD, calibrator

Vitros by Ortho-Clinical Diagnostics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

DEN210040 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 81de111c-7b42-46d4-954b-8160abc4d84e 36 fields · synced May 30, 2026