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STERIKING® CombiWrap 10

EUDAMED

Class I (EU MDR)

Ref CW10120Ref CW10100

by Wipak Oy

Identity

Trade Name
STERIKING® CombiWrap 10 EUDAMED
Device Name
STERIKING® Wraps EUDAMED
Model / Reference
CW10120 EUDAMED
CW10100 EUDAMED

Identifiers

Primary DI / UDI-DI
06438263919922 EUDAMED
06438263919915 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 10 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 87a227bd-c71f-4420-b6f0-60be01f56899 61 fields · synced Aug 3, 2026
  • EUDAMED 43a6181b-f062-42f6-8a5d-9e98ad30143e 61 fields · synced May 17, 2026