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Quest Diagnostics

FDA UDI

Class I (US FDA UDI)

by Bio-Rad Laboratories

Identity

Trade Name
Quest Diagnostics FDA UDI
Generic Name
Multiple clinical chemistry protein IVD, control FDA UDI
Device Name
Quest Diagnostics Immunoassay/TDM Control (A human serum immunoassay/TDM control.) FDA UDI
Model / Reference
930 FDA UDI
Description
Quest Diagnostics Immunoassay/TDM Control (A human serum immunoassay/TDM control.) FDA UDI

Identifiers

Catalog Number
930 FDA UDI
Primary DI / UDI-DI
03610520540916 FDA UDI
510(k) Number
K050536 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multiple clinical chemistry protein IVD, control

Quest Diagnostics 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

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Manufacturer

Sources (1)

  • FDA UDI e61d424a-c4e7-48be-a45c-9d511f47f052 36 fields · synced Jun 6, 2026