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Berofine

EUDAMED

Class IIa (EU MDR)

Ref 900536B

by Beromed GmbH Hospital Products

Identity

Trade Name
BEROFINE EUDAMED
Device Name
BEROFINE hypodermic needle EUDAMED
Model / Reference
900536B EUDAMED

Identifiers

Primary DI / UDI-DI
24032731900533 EUDAMED
Basic UDI-DI
4032731G10-01IIaEL EUDAMED
EMDN Code
A0101010102 HYPODERMIC SYRINGE NEEDLES, W/O SAFETY SYSTEMS EUDAMED

Classification

Device Class
Class IIa EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Berofine by Beromed GmbH Hospital Products — Class IIa — CE/MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
DE-MF-000007458

Sources (1)

  • EUDAMED 7985a5c6-1b83-4167-a887-2cee7b14862f 61 fields · synced Oct 6, 2026