Identity
- Trade Name
- ADITUS BALLOON CATHETER EUDAMED
- Device Name
- ADITUS BALLOON CATHETER EUDAMEDKYPHOPLASTY SYSTEMS EUDAMED
- Model / Reference
- AKB20J EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08033860033958 EUDAMED
- Basic UDI-DI
- B-08033860033958 EUDAMED8033860KYPFT05A9T EUDAMED
- EMDN Code
- K010301 SPINAL PERCUTANEOUS PLASTIC DEVICES WITH BALLOON EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Italy EUDAMED
Clinical & Handling
Sterile
Yes
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
Aditus Balloon Catheter by Biopsybell Srl — Class IIa — MDR, MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | B-08033860033958 | Class IIa | Active |
| EUDAMED | European Union | CE/MDD | B-08033860033958 | Class IIa | Active |
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Manufacturer
- Manufacturer
- Biopsybell Srl
- EUDAMED SRN
- IT-MF-000011601
Sources (2)
- EUDAMED 2b6cd01c-a60b-422a-962d-c2d08c548c4f 61 fields · synced Jul 19, 2026
- EUDAMED 3dbc1cb7-f8a4-4992-ac9a-41a8cd5c205e 61 fields · synced May 19, 2026