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CEDIA Buprenorphine Controls

EUDAMEDFDA UDI

Class IVD General (EU MDR)

Ref 100246

by Microgenics Corporation

Identity

Trade Name
CEDIA Buprenorphine Controls FDA UDI
Generic Name
Buprenorphine IVD, control FDA UDI
Device Name
CEDIA Buprenorphine Controls EUDAMED
Model / Reference
100246 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
00884883001756 EUDAMEDFDA UDI
Basic UDI-DI
B-00884883001756 EUDAMED
FDA Product Code
LAS FDA UDI
EMDN Code
W0102090117 BUPRENORPHINE EUDAMED
GMDN Term
Buprenorphine IVD, control FDA UDI

Classification

Device Class
Class IVD General EUDAMED
Class I FDA UDI
Regulation Number
862.3280 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

Yes

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

CEDIA Buprenorphine Controls by Microgenics Corporation — Class IVD General — IVDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDD

United States Pending data

FDA UDI

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Manufacturer

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

Sources (2)

  • EUDAMED 6e65f236-4e92-4af4-9d8f-489e3686b476 61 fields · synced Jun 19, 2026
  • FDA UDI 819b0504-d256-438c-a645-9cac0cefa7bf 32 fields · synced May 30, 2026