← Back to catalogue

Vitros

FDA UDI

Class I (US FDA UDI)

by Ortho-Clinical Diagnostics

Identity

Trade Name
VITROS FDA UDI
Generic Name
Multiple reproductive health marker IVD, control FDA UDI
Device Name
VITROS Immunodiagnostic Products RE Controls FDA UDI
Model / Reference
1009406 FDA UDI
Description
VITROS Immunodiagnostic Products RE Controls FDA UDI

Identifiers

Catalog Number
1009406 FDA UDI
Primary DI / UDI-DI
10758750008322 FDA UDI
FDA Product Code
JJY FDA UDI
GMDN Term
Multiple reproductive health marker IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1660 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

No

FDA UDI

Category: Multiple reproductive health marker IVD, control

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

Similar devices

Also classified as Multiple reproductive health marker IVD, control.

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 f651e652-1951-4c9f-b275-0298dc7a9a6c 35 fields · synced May 30, 2026