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STERIKING® See-Through Gusseted Rolls

EUDAMED

Class I (EU MDR)

Ref RB50; RB50-3P

by Wipak Oy

Identity

Trade Name
STERIKING® See-Through Gusseted Rolls EUDAMED
Device Name
STERIKING® Pouches and Rolls EUDAMED
Model / Reference
RB50; RB50-3P EUDAMED

Identifiers

Primary DI / UDI-DI
06438263650092 EUDAMED
Basic UDI-DI
6438263ST14010NK EUDAMED
EMDN Code
S01020102 STERILISATION REELS, GUSSETED, PAPER/PLASTIC FILM 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® See-Through Gusseted Rolls 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 b8121f85-a772-4cf2-bbe6-2d43543f4281 61 fields · synced Jun 19, 2026
  • EUDAMED b8121f85-a772-4cf2-bbe6-2d43543f4281-1 61 fields · synced Jun 10, 2026