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Rti-Inj

EUDAMED

Class I (EU MDR)

Ref RTI-INJ

by Biopsybell Srl

Identity

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

Identifiers

Primary DI / UDI-DI
08033860031558 EUDAMED
Basic UDI-DI
8033860KYPFT05A1S3Z EUDAMED
B-08033860031558 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-Inj 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 637b14f7-84e3-4d10-b95e-90f123f9f321 61 fields · synced Jul 9, 2026
  • EUDAMED bb0167dc-0bd4-471c-b462-c304799d8ccf 61 fields · synced Jul 9, 2026