← Back to catalogue

Dopamine ELISA

FDA UDI

Class I (US FDA UDI)

by DRG Instruments Gesellschaft mit beschränkter Haftung

Identity

Trade Name
Dopamine ELISA FDA UDI
Generic Name
Multiple biogenic amine neurotransmitter IVD, reagent FDA UDI
Device Name
Enzyme Immunoassay for the quantitative determination of dopamine in plasma and urine. FDA UDI
Model / Reference
EIA-4161 FDA UDI
Description
Enzyme Immunoassay for the quantitative determination of dopamine in plasma and urine. FDA UDI

Identifiers

Catalog Number
EIA-4161 FDA UDI
Primary DI / UDI-DI
04048474041613 FDA UDI
FDA Product Code
CHQ FDA UDI
GMDN Term
Multiple biogenic amine neurotransmitter IVD, reagent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1165 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dopamine ELISA by DRG Instruments Gesellschaft mit beschränkter Haftung — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 851da935-1c9d-413c-8d8e-0eef5525ea01 37 fields · synced Jun 8, 2026