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Splinty S

EUDAMED

Class I (EU MDR)

Ref MKK-SL-S

by Human Protection BV

Identity

Trade Name
Splinty S EUDAMED
Device Name
Splints EUDAMED
Model / Reference
MKK-SL-S EUDAMED

Identifiers

Primary DI / UDI-DI
08719325611243 EUDAMED
Basic UDI-DI
8719325475SL001AS EUDAMED
Direct Marketing DI
08719325611243 EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands 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

Splinty S by Human Protection BV — 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
Human Protection BV
EUDAMED SRN
NL-MF-000002013

Sources (1)

  • EUDAMED 241c7937-06e4-450c-ad7f-b487c11e5cbd 61 fields · synced Jun 19, 2026