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Werosalin

EUDAMED

Class IIa (EU MDR)

Ref 51068Ref 51066

by Naturelle Consumer Products

Identity

Trade Name
Werosalin EUDAMED
Device Name
Sterile Saline Wound Cleansing Wipe EUDAMED
Model / Reference
51068 EUDAMED
51066 EUDAMED

Identifiers

Primary DI / UDI-DI
05017599001894 EUDAMED
15017599001891 EUDAMED
Basic UDI-DI
5017599000TF11WN EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED
Z12019003 WOUND TREATMENT EQUIPMENT EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

Werosalin 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 (2)

  • EUDAMED 8a2ad5c8-0e73-4022-9f6a-17409d174828 61 fields · synced Oct 6, 2026
  • EUDAMED 82f172f2-0f41-42bd-b183-e7d1b228a6d5 61 fields · synced May 19, 2026