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CEDIA DAU Barbiturate Assay

FDA UDIEUDAMED

Class II (US FDA UDI)

by Microgenics Corporation

Identity

Trade Name
CEDIA DAU Barbiturate Assay FDA UDI
Generic Name
Barbiturate IVD, kit, enzyme immunoassay (EIA) FDA UDI
Model / Reference
1661213 FDA UDI

Identifiers

Primary DI / UDI-DI
00884883004092 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

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

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)

CEDIA DAU Barbiturate Assay by Microgenics Corporation — Class II — IVDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

IVDD

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 59b40d69-9f83-4b5c-9498-23f6389853f2 32 fields · synced Jun 9, 2026
  • EUDAMED 1 fields · synced May 28, 2026