← Back to catalogue

InteliQ

FDA UDI

Class I (US FDA UDI)

by Bio-Rad Laboratories

Identity

Trade Name
InteliQ FDA UDI
Generic Name
Multiple clinical chemistry protein IVD, control FDA UDI
Device Name
InteliQ Immunoassay Plus Control Level 2 (A human serum assayed immunoassay and TDM control.) FDA UDI
Model / Reference
12009949 FDA UDI
Description
InteliQ Immunoassay Plus Control Level 2 (A human serum assayed immunoassay and TDM control.) FDA UDI

Identifiers

Catalog Number
12009949 FDA UDI
Primary DI / UDI-DI
03610522114191 FDA UDI
FDA Product Code
JJY FDA UDI
GMDN Term
Multiple clinical chemistry protein 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 clinical chemistry protein IVD, control

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

Similar devices

Also classified as Multiple clinical chemistry protein 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 7426c9cd-b7e6-4950-b40d-e97b22461731 36 fields · synced May 30, 2026