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Vitros

FDA UDI

Class N (US FDA UDI)

by Ortho-Clinical Diagnostics

Identity

Trade Name
VITROS FDA UDI
Generic Name
SARS-CoV-2 total antibody IVD, control FDA UDI
Device Name
VITROS Immunodiagnostic Products Anti-SARS-COV-2 Total Controls FDA UDI
Model / Reference
6199924 FDA UDI
Description
VITROS Immunodiagnostic Products Anti-SARS-COV-2 Total Controls FDA UDI

Identifiers

Catalog Number
6199924 FDA UDI
Primary DI / UDI-DI
10758750033409 FDA UDI
FDA Product Code
QKO FDA UDI
QVP FDA UDI
GMDN Term
SARS-CoV-2 total antibody IVD, control FDA UDI

Classification

Device Class
N 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

Yes

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, control

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

Similar devices

Also classified as SARS-CoV-2 total antibody IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ortho-Clinical Diagnostics

Sources (1)

  • FDA UDI 5fad91e9-8b8e-4573-8ee4-2fe07f18ca68 35 fields · synced May 30, 2026