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Validate

FDA UDI

Class I (US FDA UDI)

by LGC Clinical Diagnostics, Inc.

Identity

Trade Name
Validate FDA UDI
Generic Name
Multiple-type clinical chemistry analyte profile IVD, control FDA UDI
Device Name
Validate GC1ab is intended for the quantitative determination of Calibration Verification/Linearity of general chemistries on automated instruments. FDA UDI
Model / Reference
1100ab FDA UDI
Description
Validate GC1ab is intended for the quantitative determination of Calibration Verification/Linearity of general chemistries on automated instruments. FDA UDI

Identifiers

Catalog Number
1100ab FDA UDI
Primary DI / UDI-DI
00859110005180 FDA UDI
FDA Product Code
JJY FDA UDI
GMDN Term
Multiple-type clinical chemistry analyte profile 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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: Multiple-type clinical chemistry analyte profile IVD, control

Validate by LGC Clinical Diagnostics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple-type clinical chemistry analyte profile IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e2c9db37-2e7f-46c9-a84d-760b62089c93 37 fields · synced Jun 9, 2026