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Cifopack Drill

EUDAMED

Class IIa (EU MDR)

Ref KPA08-DRI

by Biopsybell Srl

Identity

Trade Name
CIFOPACK DRILL EUDAMED
Device Name
KYPHOPLASTY SYSTEMS EUDAMED
CIFOPACK DRILL EUDAMED
Model / Reference
KPA08-DRI EUDAMED

Identifiers

Primary DI / UDI-DI
08033860035891 EUDAMED
Basic UDI-DI
8033860KYPFT05A9T EUDAMED
B-08033860035891 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 Drill 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 ebbc4614-86b2-488e-87f0-8d9af32b2459 61 fields · synced Jul 9, 2026
  • EUDAMED b1c910e1-9b72-4831-9aa8-c8a617d0f56c 61 fields · synced May 17, 2026