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LDH Liqui-UV®

FDA UDI

Class II (US FDA UDI)

by Stanbio Laboratory, L.p.

Identity

Trade Name
LDH Liqui-UV® FDA UDI
Generic Name
Total lactate dehydrogenase (LDH) IVD, kit, spectrophotometry FDA UDI
Device Name
For the Quantitative Determination of Lactate Dehydrogenase in Serum and EDTA Plasma. FDA UDI
Model / Reference
2940-430 FDA UDI
Description
For the Quantitative Determination of Lactate Dehydrogenase in Serum and EDTA Plasma. FDA UDI

Identifiers

Catalog Number
2940-430 FDA UDI
Primary DI / UDI-DI
00657498000946 FDA UDI
FDA Product Code
CFJ FDA UDI
GMDN Term
Total lactate dehydrogenase (LDH) IVD, kit, spectrophotometry FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1440 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

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: Total lactate dehydrogenase (LDH) IVD, kit, spectrophotometry

LDH Liqui-UV® by Stanbio Laboratory, L.p. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total lactate dehydrogenase (LDH) IVD, kit, spectrophotometry.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stanbio Laboratory, L.p.

Sources (1)

  • FDA UDI ce532b88-d768-4baf-8db3-d344f8ead318 36 fields · synced May 31, 2026