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Ago 25GX 5/8"- PENTALANCE

EUDAMED

Class IIa (EU MDR)

Ref 004021H58

by Pentaferte Italia Srl

Identity

Trade Name
Ago 25GX 5/8"- PENTALANCE EUDAMED
Device Name
SIRINGHE CON AGO E AGHI IPODERMICI EUDAMED
Model / Reference
004021H58 EUDAMED

Identifiers

Primary DI / UDI-DI
08015262009922 EUDAMED
Basic UDI-DI
80152621034S EUDAMED
EMDN Code
A0101010102 HYPODERMIC SYRINGE NEEDLES, W/O SAFETY SYSTEMS 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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Ago 25GX 5/8"- PENTALANCE by Pentaferte Italia Srl — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
IT-MF-000040982

Sources (1)

  • EUDAMED 69f32d19-a3d5-424c-a68a-46c07afd0f0e 61 fields · synced Oct 6, 2026