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CEDIA Benzodiazepine Assay

EUDAMEDFDA UDIFDA 510(k)

Class IVD General (EU MDR)

Ref 100085510(k) K190968

by Microgenics Corporation

Identity

Trade Name
CEDIA Benzodiazepine Assay FDA UDI
Generic Name
Benzodiazepine group IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
CEDIA Benzodiazepine Assay EUDAMED
Model / Reference
100085 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
00884883001428 EUDAMEDFDA UDI
Basic UDI-DI
B-00884883001428 EUDAMED
FDA Product Code
JXM FDA UDI
EMDN Code
W0102090104 BENZODIAZEPINES EUDAMED
GMDN Term
Benzodiazepine group IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class IVD General EUDAMED
Class II FDA UDI
Regulation Number
862.3170 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

Yes

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

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

CEDIA Benzodiazepine Assay by Microgenics Corporation — Class IVD General — FDA_510K, IVDD — listed in EUDAMED, FDA GUDID, FDA 510(k)

Authorization Coverage (2 countries)

Regulatory Authorizations

United States Active

FDA_510K

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
US-MF-000030375
Authorised Representative
B·R·A·H·M·S GmbH DE-AR-000026031

Sources (3)

  • EUDAMED 3d558b7c-09d1-4d10-8489-dbfef13238a7 85 fields · synced Jun 18, 2026
  • FDA UDI 1d17a7fe-7132-47dd-9ae4-99b726963a7a 32 fields · synced May 29, 2026
  • FDA 510(k) K190968 1 fields · synced May 18, 2026