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Aditus Syringe

EUDAMED

Class I (EU MDR)

Ref AKSI25

by Biopsybell Srl

Identity

Trade Name
ADITUS SYRINGE EUDAMED
Device Name
ACCESSORIES FOR BONE AUGMENTATION MATERIAL INJECTION EUDAMED
Model / Reference
AKSI25 EUDAMED

Identifiers

Primary DI / UDI-DI
08033860033972 EUDAMED
Basic UDI-DI
8033860KYPFT05A1S3Z EUDAMED
EMDN Code
P099002 ORTHOPAEDIC CEMENT PREPARATION AND APPLICATION DEVICES AND KITS EUDAMED

Classification

Device Class
Class I 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 Syringe by Biopsybell Srl — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Biopsybell Srl
EUDAMED SRN
IT-MF-000011601

Sources (1)

  • EUDAMED a004f149-04c8-4c3b-94de-440ff0b0e672 61 fields · synced Aug 1, 2026