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Renova Spine Kyphoplasty Working Cannula And Diamond Tip

EUDAMED

Class IIa (EU MDR)

Ref RESWD0812C

by Biopsybell Srl

Identity

Trade Name
RENOVA SPINE KYPHOPLASTY WORKING CANNULA AND DIAMOND TIP EUDAMED
Device Name
KYPHOPLASTY SYSTEMS EUDAMED
RENOVA SPINE KYPHOPLASTY WORKING CANNULA AND DIAMOND TIP EUDAMED
Model / Reference
RESWD0812C EUDAMED

Identifiers

Primary DI / UDI-DI
08033860019068 EUDAMED
Basic UDI-DI
8033860KYPFT05A9T EUDAMED
B-08033860019068 EUDAMED
EMDN Code
K010301 SPINAL PERCUTANEOUS PLASTIC DEVICES WITH BALLOON 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

Renova Spine Kyphoplasty Working Cannula And Diamond Tip by Biopsybell Srl — Class IIa — 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 f672a696-6c24-4ac3-bc46-919aa72096a5 61 fields · synced Aug 4, 2026
  • EUDAMED d0673f29-90ae-4d73-a78f-efbec84821bf 61 fields · synced Aug 4, 2026