Neoprene Bandage

by Bevaplast B.V. 24 variants

Ref 6987

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number8712175_TD_11_BRACE57 Basic UDI-DI 08710198301194UDI-DI	Date14 Feb 2025Registered	StatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name: Neoprene Bandage
Model / Reference: 6987

Primary DI / UDI-DI: 08710198301194
Basic UDI-DI: 8712175_TD_11_BRACE57
Direct Marketing DI: 08710198301194
EMDN Code: M030499 Elastic bandages, support and compression - other

Device Class: Class I
EU market of registration: Netherlands

Manufacturer details

EUDAMED SRN: NL-MF-000004386

Other devices from Bevaplast B.V.

Wound Plaster

Class I
No

Class I
Kinesiology Tape

Class I
Cohesive Bandage

Class I
Corn Ring

Class I
First Aid Kit(s)

Class IIa

See all devices from Bevaplast B.V. →

Properties

Other properties (13)

Sterile: No
Implantable: No
Reusable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No