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Neoprene Bandage

EUDAMED

Class I (EU MDR)

Ref 8614 / 8821

by Bevaplast B.V.

Identity

Device Name
Neoprene Bandage EUDAMED
Model / Reference
8614 / 8821 EUDAMED

Identifiers

Primary DI / UDI-DI
08712175940761 EUDAMED
Basic UDI-DI
8712175_TD_11_BRACE57 EUDAMED
Direct Marketing DI
08712175940761 EUDAMED
EMDN Code
M030499 ELASTIC BANDAGES, SUPPORT AND COMPRESSION - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands 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

Category: Compression/pressure sock/stocking, reusable

Neoprene Bandage by Bevaplast B.V. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Compression/pressure sock/stocking, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Bevaplast B.V.
EUDAMED SRN
NL-MF-000004386

Sources (1)

  • EUDAMED 720faf78-ceb2-4ed0-87a0-02b4ea13e36d 61 fields · synced Jun 18, 2026