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AmpliTrol

FDA UDI

Class I (US FDA UDI)

by Bio-Rad Laboratories

Identity

Trade Name
AmpliTrol FDA UDI
Generic Name
Multiple-type sexually transmitted pathogen nucleic acid IVD, control FDA UDI
Device Name
AmpliTrol CT/GC (An unassayed C. trachomatis and N. gonorrhoeae nucleic acid control.) FDA UDI
Model / Reference
00126 FDA UDI
Description
AmpliTrol CT/GC (An unassayed C. trachomatis and N. gonorrhoeae nucleic acid control.) FDA UDI

Identifiers

Catalog Number
00126 FDA UDI
Primary DI / UDI-DI
00847661002772 FDA UDI
FDA Product Code
OHQ FDA UDI
GMDN Term
Multiple-type sexually transmitted pathogen nucleic acid 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

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

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

No

FDA UDI

Category: Multiple-type sexually transmitted pathogen nucleic acid IVD, control

AmpliTrol by Bio-Rad Laboratories — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple-type sexually transmitted pathogen nucleic acid IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bio-Rad Laboratories

Sources (1)

  • FDA UDI 6e3f039c-3c3c-4b1c-827a-d96bb02f7fab 36 fields · synced May 30, 2026