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Renova Spine Classic Access System

EUDAMED

Class IIa (EU MDR)

Ref RES0812002L

by Biopsybell Srl

Identity

Trade Name
RENOVA SPINE CLASSIC ACCESS SYSTEM EUDAMED
Device Name
KYPHOPLASTY SYSTEMS EUDAMED
RENOVA SPINE CLASSIC ACCESS SYSTEM EUDAMED
Model / Reference
RES0812002L EUDAMED

Identifiers

Primary DI / UDI-DI
08033860010805 EUDAMED
Basic UDI-DI
8033860KYPFT05A9T EUDAMED
B-08033860010805 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 Classic Access System 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 a2e6c83b-5e70-4700-a95b-ae1c2088feaa 61 fields · synced Jul 16, 2026
  • EUDAMED 35a5e66a-6a02-4916-b1a4-e34f87d31fe2 61 fields · synced May 19, 2026