← Back to catalogue

Rti-K

EUDAMED

Class IIa (EU MDR)

Ref RTI-KDC6

by Biopsybell Srl

Identity

Trade Name
RTI-K EUDAMED
Device Name
KYPHOPLASTY SYSTEMS EUDAMED
Model / Reference
RTI-KDC6 EUDAMED

Identifiers

Primary DI / UDI-DI
08033860031817 EUDAMED
Basic UDI-DI
8033860KYPFT05A9T EUDAMED
EMDN Code
A019011 INTRAOSSEOUS INFUSION AND VERTEBROPLASTY INFUSION NEEDLES AND KITS 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

Category: Intraosseous infusion kit

Rti-K by Biopsybell Srl — Class IIa — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Biopsybell Srl
EUDAMED SRN
IT-MF-000011601

Sources (1)

  • EUDAMED d16d0c33-bdd6-4934-8876-8b0612b552c3 61 fields · synced Jun 18, 2026