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Barbiturate Enzyme Immunoassay

FDA UDI

Class II (US FDA UDI)

by Lin-Zhi International, Inc.

Identity

Trade Name
Barbiturate Enzyme Immunoassay FDA UDI
Generic Name
Barbiturate IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
Large Test Kit. Antibody/Substrate Reagent (R1): 1000 mL. Enzyme Conjugate Reagent (R2): 375 mL. FDA UDI
Model / Reference
0141 FDA UDI
Description
Large Test Kit. Antibody/Substrate Reagent (R1): 1000 mL. Enzyme Conjugate Reagent (R2): 375 mL. FDA UDI

Identifiers

Catalog Number
0141 FDA UDI
Primary DI / UDI-DI
B07601410 FDA UDI
510(k) Number
K032764 FDA UDI
FDA Product Code
DIS FDA UDI
GMDN Term
Barbiturate IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3150 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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: Barbiturate IVD, kit, enzyme immunoassay (EIA)

Barbiturate Enzyme Immunoassay by Lin-Zhi International, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Barbiturate IVD, kit, enzyme immunoassay (EIA).

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0a14ef3e-2c53-47fe-a352-7e17aaf2ab02 36 fields · synced Jun 9, 2026