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BRS® (Biofilm-Removing-Set)

EUDAMED

Class I (EU MDR)

Ref 3215

by Alpro Medical Gmbh

Identity

Trade Name
BRS® (Biofilm-Removing-Set) EUDAMED
Device Name
BRS® (Biofilm-Removing-Set) EUDAMED
Model / Reference
3215 EUDAMED

Identifiers

Primary DI / UDI-DI
+E25132151 EUDAMED
Basic UDI-DI
++E251013209009L EUDAMED
Direct Marketing DI
+E25132151 EUDAMED
EMDN Code
V0799 PRODUCTS FOR CLEANING MEDICAL DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

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

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

BRS® (Biofilm-Removing-Set) by Alpro Medical Gmbh — Class I — 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

Manufacturer
Alpro Medical Gmbh
EUDAMED SRN
DE-MF-000010603

Sources (1)

  • EUDAMED d5fca59a-8d1d-4aa9-9bd1-57445b1cf781 61 fields · synced Oct 7, 2026