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Vitros

FDA UDI

Class II (US FDA UDI)

by Ortho-Clinical Diagnostics

Identity

Trade Name
VITROS FDA UDI
Generic Name
Gentamicin therapeutic drug monitoring IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
VITROS Chemistry Products GENT Reagent FDA UDI
Model / Reference
6801711 FDA UDI
Description
VITROS Chemistry Products GENT Reagent FDA UDI

Identifiers

Catalog Number
6801711 FDA UDI
Primary DI / UDI-DI
10758750006755 FDA UDI
FDA Product Code
LCD FDA UDI
GMDN Term
Gentamicin therapeutic drug monitoring IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3450 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: Gentamicin therapeutic drug monitoring IVD, kit, enzyme immunoassay (EIA)

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

Similar devices

Also classified as Gentamicin therapeutic drug monitoring IVD, kit, enzyme immunoassay (EIA).

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 d33a3d2d-4737-45c1-9bb2-9891bd856a6a 35 fields · synced May 30, 2026