← Back to catalogue

Neoprene Bandage

EUDAMED

Class I (EU MDR)

Ref 8638 / 8837

by Bevaplast B.V.

Identity

Device Name
Neoprene Bandage EUDAMED
Model / Reference
8638 / 8837 EUDAMED

Identifiers

Primary DI / UDI-DI
08712175940846 EUDAMED
Basic UDI-DI
8712175_TD_11_BRACE57 EUDAMED
Direct Marketing DI
08712175940846 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

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

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED d10168fe-0f8d-4bba-ae3f-f499919e6f3c 61 fields · synced Jun 19, 2026