← Back to catalogue

Waldberg

EUDAMED

Class IIa (EU MDR)

Ref W1012Model G1302s

by Zhejiang Longterm Medical Technology Co., Ltd.

Identity

Trade Name
WALDBERG EUDAMED
Device Name
Hydrocolloid blister plaster EUDAMED
Model / Reference
G1302s EUDAMED
W1012 EUDAMED

Identifiers

Primary DI / UDI-DI
03401053750121 EUDAMED
Basic UDI-DI
69263655200147Z EUDAMED
EMDN Code
M04040301 HYDROCOLLOID DRESSINGS, NON-COMBINED EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

Yes

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

Waldberg by Zhejiang Longterm Medical Technology Co., Ltd. — Class IIa — 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-000001161
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 4fc560e9-682e-4401-944f-e4bbd4265ed8 61 fields · synced Jul 20, 2026