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Sterowipe

EUDAMED

Class IIa (EU MDR)

Ref 9021B

by Naturelle Consumer Products

Identity

Trade Name
Sterowipe EUDAMED
Device Name
Sterile Saline Wound Cleansing Wipe EUDAMED
Model / Reference
9021B EUDAMED

Identifiers

Primary DI / UDI-DI
05020581296314 EUDAMED
Basic UDI-DI
5017599000TF11WN EUDAMED
Direct Marketing DI
05020581296314 EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Northern Ireland 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

Category: Device sterilization/disinfection container, reusable

Sterowipe by Naturelle Consumer Products — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
XI-MF-000018016

Sources (1)

  • EUDAMED f4454e68-3d8e-44ea-9eb8-e879e760a74b 61 fields · synced Oct 6, 2026