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Rti-Mx

EUDAMED

Class I (EU MDR)

Ref RTI-MX

by Biopsybell Srl

Identity

Trade Name
RTI-MX EUDAMED
Device Name
ACCESSORIES FOR BONE AUGMENTATION MATERIAL INJECTION EUDAMED
RTI-MX EUDAMED
Model / Reference
RTI-MX EUDAMED

Identifiers

Primary DI / UDI-DI
08033860031534 EUDAMED
Basic UDI-DI
8033860KYPFT05A1S3Z EUDAMED
B-08033860031534 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

Rti-Mx by Biopsybell Srl — Class I — MDD, MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Biopsybell Srl
EUDAMED SRN
IT-MF-000011601

Sources (2)

  • EUDAMED 7a8fbd4b-f50e-4632-a0ec-14951746bba1 61 fields · synced Sep 18, 2026
  • EUDAMED e778a6ee-7318-4d40-ab93-3ba850dfb9e4 61 fields · synced Sep 18, 2026