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9113-5 L

EUDAMED

Class I (EU MDR)

Ref 9113-5 L

by Voe , S.a

Identity

Trade Name
9113-5 L EUDAMED
Device Name
STANDARD COMPRESSION BURNS GARMENT EUDAMED
Model / Reference
9113-5 L EUDAMED

Identifiers

Primary DI / UDI-DI
08435353320437 EUDAMED
Basic UDI-DI
84353533BURNSR3 EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Spain 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

Category: Device sterilization/disinfection container, reusable

9113-5 L by Voe , S.a — Class I — 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

Manufacturer
Voe , S.a
EUDAMED SRN
ES-MF-000013290

Sources (1)

  • EUDAMED 6fc0aeea-f168-401f-9eea-e38347a8b824 61 fields · synced Jul 21, 2026