← Back to catalogue

Woundplast

EUDAMED

Class I (EU MDR)

Ref WLD6013Model WLD6013;1.9cmx7.2cm、9cmx15cm;or as per required

by Hubei Wanli Protective Products Co., Ltd.

Identity

Device Name
Woundplast EUDAMED
Model / Reference
WLD6013;1.9cmx7.2cm、9cmx15cm;or as per required EUDAMED
WLD6013 EUDAMED

Identifiers

Primary DI / UDI-DI
06973888826595 EUDAMED
Basic UDI-DI
697388882WLD60138F EUDAMED
EMDN Code
M0599 MEDICAL PLASTERS - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria 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

Woundplast by Hubei Wanli Protective Products Co., Ltd. — 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

EUDAMED SRN
CN-MF-000008182
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED 3c9823e4-ad76-4207-b948-123faa378f79 61 fields · synced Oct 7, 2026