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Rti-Mis

EUDAMED

Class IIa (EU MDR)

Ref RTI-MISG1315BP

by Biopsybell Srl

Identity

Trade Name
RTI-MIS EUDAMED
Device Name
CEMENT INJECTION SYSTEMS FOR MINI-INVASIVE BONE SURGERY EUDAMED
Model / Reference
RTI-MISG1315BP EUDAMED

Identifiers

Primary DI / UDI-DI
08033860032005 EUDAMED
Basic UDI-DI
8033860SFFT01CU2 EUDAMED
EMDN Code
A018003 NEEDLE INTRODUCERS 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

Rti-Mis by Biopsybell Srl — Class IIa — 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 7400c41a-39e0-436a-b583-4187b957d369 61 fields · synced Jun 19, 2026