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0me2130

EUDAMED

Class IIa (EU MDR)

Ref 0ME2130Model Ago monouso per agoaspirazione

by Biomedical S.r.l.

Identity

Trade Name
0ME2130 EUDAMED
Device Name
Ago monouso Chiba per aspirati citologici EUDAMED
Model / Reference
Ago monouso per agoaspirazione EUDAMED
0ME2130 EUDAMED

Identifiers

Primary DI / UDI-DI
08053670914544 EUDAMED
Basic UDI-DI
B-08053670914544 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Diskectomy system, percutaneous, automatic

0me2130 by Biomedical S.r.l. — Class IIa — 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/MDD

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Manufacturer

Manufacturer
Biomedical S.r.l.
EUDAMED SRN
IT-MF-000027821

Sources (1)

  • EUDAMED 57d55a7f-a156-4fb3-901d-232b3a4733a6 61 fields · synced Jun 19, 2026