← Back to catalogue

Chibell

EUDAMED

Class IIa (EU MDR)

Ref CH2315EC

by Biopsybell Srl

Identity

Trade Name
CHIBELL EUDAMED
Device Name
NEEDLES FOR BIOPSY OR EXPLANT EUDAMED
CHIBELL EUDAMED
Model / Reference
CH2315EC EUDAMED

Identifiers

Primary DI / UDI-DI
08033860004095 EUDAMED
Basic UDI-DI
8033860BIOEFT01U5 EUDAMED
B-08033860004095 EUDAMED
EMDN Code
A01020102 ASPIRATION FINE 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: Diskectomy system, percutaneous, automatic

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

Similar devices

Also classified as Diskectomy system, percutaneous, automatic.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

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

Manufacturer

Manufacturer
Biopsybell Srl
EUDAMED SRN
IT-MF-000011601

Sources (2)

  • EUDAMED 1076136b-2ec5-4584-941c-ab112b90a8af 61 fields · synced Jul 23, 2026
  • EUDAMED 1e6935ca-5cad-44c8-af15-5665069b3363 61 fields · synced May 16, 2026