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SafeR Sting

EUDAMED

Class IIa (EU MDR)

Ref SFN3013Model SFN2038

by Roncadelle Operations Srl

Identity

Trade Name
SafeR Sting EUDAMED
Device Name
SafeR Sting EUDAMED
Model / Reference
SFN2038 EUDAMED
SFN3013 EUDAMED

Identifiers

Primary DI / UDI-DI
08056999020231 EUDAMED
Basic UDI-DI
805699902StingCP002000177 EUDAMED
EMDN Code
A0101010101 HYPODERMIC SYRINGE NEEDLES, WITH 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

SafeR Sting by Roncadelle Operations 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-000017979

Sources (1)

  • EUDAMED 6d8c1c51-353b-49ee-a8c2-abd2f7b37256 61 fields · synced Jun 8, 2026