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CEDIA Buprenorphine 50 ng/mL Calibrator

EUDAMEDFDA UDI

Class IVD General (EU MDR)

Ref 100244

by Microgenics Corporation

Identity

Trade Name
CEDIA Buprenorphine 50 ng/mL Calibrator FDA UDI
Generic Name
Buprenorphine IVD, calibrator FDA UDI
Device Name
CEDIA Buprenorphine 50 ng/mL Calibrator EUDAMED
Model / Reference
100244 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
00884883001732 EUDAMEDFDA UDI
Basic UDI-DI
B-00884883001732 EUDAMED
FDA Product Code
DLJ FDA UDI
EMDN Code
W0102090117 BUPRENORPHINE EUDAMED
GMDN Term
Buprenorphine IVD, calibrator FDA UDI

Classification

Device Class
Class IVD General EUDAMED
Class II FDA UDI
Regulation Number
862.3200 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 50 ng/mL Calibrator by Microgenics Corporation — Class IVD General — IVDD, FDA UDI — listed in EUDAMED, FDA GUDID

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 3e445112-0ddd-4c95-a80a-ef4d1635f6b7 61 fields · synced Jun 18, 2026
  • FDA UDI 60aee3ae-e3ad-497c-ba29-452523f6db4c 32 fields · synced May 30, 2026