← Back to catalogue

Fidget-tub enkel, lila

EUDAMED

Class I (EU MDR)

Ref 13003

by Adaptis Spektra AB

Identity

Trade Name
Fidget-tub enkel, lila EUDAMED
Device Name
Fidget-tub enkel EUDAMED
Model / Reference
13003 EUDAMED

Identifiers

Primary DI / UDI-DI
07350142990114 EUDAMED
Basic UDI-DI
73501429913000MZ EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Sweden 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

Fidget-tub enkel, lila by Adaptis Spektra AB — 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European Union No Longer Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Adaptis Spektra AB
EUDAMED SRN
SE-MF-000025764

Sources (1)

  • EUDAMED c61791a5-1040-40d4-96fd-7dcdbea48826 61 fields · synced Jul 26, 2026