← Back to catalogue

Liquichek

FDA UDI

Class II (US FDA UDI)

by Bio-Rad Laboratories

Identity

Trade Name
Liquichek FDA UDI
Generic Name
Double stranded DNA antibody (anti-dsDNA) IVD, control FDA UDI
Device Name
Liquichek Anti-nDNA Control, Positive (A pre-diluted human serum autoimmune control.) FDA UDI
Model / Reference
119 FDA UDI
Description
Liquichek Anti-nDNA Control, Positive (A pre-diluted human serum autoimmune control.) FDA UDI

Identifiers

Catalog Number
119 FDA UDI
Primary DI / UDI-DI
00847661000181 FDA UDI
FDA Product Code
DHN FDA UDI
GMDN Term
Double stranded DNA antibody (anti-dsDNA) IVD, control FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5100 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Double stranded DNA antibody (anti-dsDNA) IVD, control

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

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 87d1c728-d4c5-4c99-ae82-41fab749edff 36 fields · synced May 30, 2026