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STERIKING® CombiWrap 2

EUDAMED

Class I (EU MDR)

Ref CW2100Ref CW2120

by Wipak Oy

Identity

Trade Name
STERIKING® CombiWrap 2 EUDAMED
Device Name
STERIKING® Wraps EUDAMED
Model / Reference
CW2100 EUDAMED
CW2120 EUDAMED

Identifiers

Primary DI / UDI-DI
06438263910615 EUDAMED
06438263910622 EUDAMED
Basic UDI-DI
6438263ST15010NS EUDAMED
EMDN Code
S010302 NON-WOVEN FABRIC FOR STERILISATION EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Finland 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

STERIKING® CombiWrap 2 by Wipak Oy — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Wipak Oy
EUDAMED SRN
FI-MF-000004496

Sources (2)

  • EUDAMED bebc3f77-f9af-4a73-9014-7aa34c1670e6 61 fields · synced Jul 18, 2026
  • EUDAMED 1607c80d-f1cb-4e29-ba7f-b4ff0bcd97fb 61 fields · synced May 18, 2026