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Cifopack Balloon Catheter

EUDAMED

Class IIa (EU MDR)

Ref KPABAL20J

by Biopsybell Srl

Identity

Trade Name
CIFOPACK BALLOON CATHETER EUDAMED
Device Name
CIFOPACK BALLOON CATHETER EUDAMED
KYPHOPLASTY SYSTEMS EUDAMED
Model / Reference
KPABAL20J EUDAMED

Identifiers

Primary DI / UDI-DI
08033860034894 EUDAMED
Basic UDI-DI
B-08033860034894 EUDAMED
8033860KYPFT05A9T 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

Cifopack Balloon Catheter by Biopsybell Srl — Class IIa — MDR, MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Biopsybell Srl
EUDAMED SRN
IT-MF-000011601

Sources (2)

  • EUDAMED 87412fc0-53ea-41b0-b54a-4d99ef751b86 61 fields · synced Jun 19, 2026
  • EUDAMED 1de1eadd-6556-4c70-ac8e-779111168171 61 fields · synced May 17, 2026