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Liquichek

FDA UDI

Class I (US FDA UDI)

by Bio-Rad Laboratories

Identity

Trade Name
Liquichek FDA UDI
Generic Name
Erythrocyte sedimentation rate (ESR) IVD, control FDA UDI
Device Name
Liquichek Sedimentation Rate Control Level 2 (A human whole blood assayed erythrocyte sedimentation rate control.) FDA UDI
Model / Reference
515 FDA UDI
Description
Liquichek Sedimentation Rate Control Level 2 (A human whole blood assayed erythrocyte sedimentation rate control.) FDA UDI

Identifiers

Catalog Number
515 FDA UDI
Primary DI / UDI-DI
00847661003106 FDA UDI
FDA Product Code
JPH FDA UDI
GMDN Term
Erythrocyte sedimentation rate (ESR) IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.6700 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: Erythrocyte sedimentation rate (ESR) IVD, control

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

Similar devices

Also classified as Erythrocyte sedimentation rate (ESR) IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 16b78edd-0a63-46b3-9b24-8d3ae0d937ac 36 fields · synced May 30, 2026