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STERIKING® CombiWrap 3

EUDAMED

Class I (EU MDR)

Ref CW3075Ref CW3100Ref CW3090

by Wipak Oy

Identity

Trade Name
STERIKING® CombiWrap 3 EUDAMED
Device Name
STERIKING® Wraps EUDAMED
Model / Reference
CW3075 EUDAMED
CW3100 EUDAMED
CW3090 EUDAMED

Identifiers

Primary DI / UDI-DI
06438263910639 EUDAMED
06438263910653 EUDAMED
06438263666109 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 3 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 (3)

  • EUDAMED 49fd764c-c32b-45c3-a0be-23145543fabb 61 fields · synced Jul 13, 2026
  • EUDAMED ac73a902-8906-48f2-a0b8-88d76a23490a 61 fields · synced May 18, 2026
  • EUDAMED a3247308-59ce-4e5b-94a0-92c6f6745cc3 61 fields · synced May 18, 2026