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Axeltyngd Formsydd, Small

EUDAMED

Class I (EU MDR)

Ref 16002

by Adaptis Spektra AB

Identity

Trade Name
Axeltyngd Formsydd, Small EUDAMED
Device Name
Axeltyngd, formsydd EUDAMED
Model / Reference
16002 EUDAMED

Identifiers

Primary DI / UDI-DI
07350142990053 EUDAMED
Basic UDI-DI
73501429916000NN EUDAMED
Direct Marketing DI
07350142990053 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

Axeltyngd Formsydd, Small 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European Union No Longer Active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

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Manufacturer

Manufacturer
Adaptis Spektra AB
EUDAMED SRN
SE-MF-000025764

Sources (1)

  • EUDAMED 40c2591f-4ce4-47bd-9dd5-92de753c2b13 61 fields · synced Jun 18, 2026