← Back to catalogue

Opiate Enzyme Immunoassay

FDA UDI

Class II (US FDA UDI)

by Lin-Zhi International, Inc.

Identity

Trade Name
Opiate Enzyme Immunoassay FDA UDI
Generic Name
Opiate/opiate metabolite 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
0021b FDA UDI
Description
Large Test Kit. Antibody/Substrate Reagent (R1): 1000 mL. Enzyme Conjugate Reagent (R2): 375 mL. FDA UDI

Identifiers

Catalog Number
0021b FDA UDI
Primary DI / UDI-DI
B0760021B0 FDA UDI
510(k) Number
K110298 FDA UDI
FDA Product Code
DJG FDA UDI
GMDN Term
Opiate/opiate metabolite IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3650 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: Opiate/opiate metabolite IVD, kit, enzyme immunoassay (EIA)

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

Similar devices

Also classified as Opiate/opiate metabolite IVD, kit, enzyme immunoassay (EIA).

Cleared under the same submission

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 774dbe92-2860-4d79-99b3-f9d761ff373d 36 fields · synced Jun 9, 2026