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Aditus Inflation Device

EUDAMED

Class IIa (EU MDR)

Ref AKA30

by Biopsybell Srl

Identity

Trade Name
ADITUS INFLATION DEVICE EUDAMED
Device Name
ADITUS INFLATION DEVICE EUDAMED
Model / Reference
AKA30 EUDAMED

Identifiers

Primary DI / UDI-DI
08033860033835 EUDAMED
Basic UDI-DI
B-08033860033835 EUDAMED
EMDN Code
V80 CLINICAL USE ACCESSORIES NOT INCLUDED IN OTHER CLASSES 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Aditus Inflation Device by Biopsybell Srl — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Biopsybell Srl
EUDAMED SRN
IT-MF-000011601

Sources (1)

  • EUDAMED d967100c-7114-4582-80a5-83492b5f1d75 61 fields · synced Jun 19, 2026