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Spinertome

EUDAMED

Class IIb (EU MDR)

Ref 5051312

by Adria S.r.l.

Identity

Trade Name
Spinertome EUDAMED
Device Name
Devices for percutaneous discectomy and motorized for vertebroplasty / kyphoplasty EUDAMED
Model / Reference
5051312 EUDAMED

Identifiers

Primary DI / UDI-DI
08053175000889 EUDAMED
Basic UDI-DI
803373711K0299VX EUDAMED
EMDN Code
A019011 INTRAOSSEOUS INFUSION AND VERTEBROPLASTY INFUSION NEEDLES AND KITS EUDAMED

Classification

Device Class
Class IIb 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

Category: Intraosseous infusion kit

Spinertome by Adria S.r.l. — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Intraosseous infusion kit.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Adria S.r.l.
EUDAMED SRN
IT-MF-000027852

Sources (1)

  • EUDAMED 9ee279a9-af28-48b4-ace3-7f64ae22bd5e 61 fields · synced Jul 17, 2026