Identity
- Trade Name
- Fidget-tub två kulor, vit EUDAMED
- Device Name
- Fidget-tub två kulor EUDAMED
- Model / Reference
- 13025 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07350142990398 EUDAMED
- Basic UDI-DI
- 73501429913020N7 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 två kulor, vit by Adaptis Spektra AB — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
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Also classified as Device sterilization/disinfection container, reusable.
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Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union No Longer Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 73501429913020N7 | Class I | No Longer Active |
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Manufacturer
- Manufacturer
- Adaptis Spektra AB
- EUDAMED SRN
- SE-MF-000025764
Sources (1)
- EUDAMED b5ae3b94-467c-4a5e-adf2-5233a5d50c0f 61 fields · synced Aug 4, 2026