MPO Felt

by Hebei Huaren Felt Co., Ltd

Ref MPO FeltModel Ⅰ、Ⅱ、Ⅲ、Ⅳ

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number697986373HRMZ2D Basic UDI-DI 06979863730000UDI-DI	Date1 Apr 2026Registered	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Withdrawn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: MPO Felt
Model / Reference: Ⅰ、Ⅱ、Ⅲ、Ⅳ, MPO Felt

Primary DI / UDI-DI: 06979863730000
Basic UDI-DI: 697986373HRMZ2D
EMDN Code: M030499 Elastic bandages, support and compression - other

Device Class: Class I
EU market of registration: Spain

Manufacturer details

EUDAMED SRN: CN-MF-000052942
Authorised representative: RIOMAVIX SOCIEDAD LIMITADA ES-AR-000001202

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