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Vitros

FDA UDI

Class II (US FDA UDI)

by Ortho-Clinical Diagnostics

Identity

Trade Name
VITROS FDA UDI
Generic Name
Total iron binding capacity (TIBC) IVD, calibrator FDA UDI
Device Name
VITROS Chemistry Products Calibrator Kit 29 FDA UDI
Model / Reference
6802344 FDA UDI
Description
VITROS Chemistry Products Calibrator Kit 29 FDA UDI

Identifiers

Catalog Number
6802344 FDA UDI
Primary DI / UDI-DI
10758750002672 FDA UDI
FDA Product Code
JIS FDA UDI
GMDN Term
Total iron binding capacity (TIBC) IVD, calibrator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1150 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: Total iron binding capacity (TIBC) IVD, calibrator

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

Similar devices

Also classified as Total iron binding capacity (TIBC) IVD, calibrator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 523c0b9c-60df-47c9-b753-988c0e9f4e0a 35 fields · synced May 30, 2026