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Mediglide

EUDAMED

Class IIa (EU MDR)

Ref SS-6092

by Romsons Group Private Limited

Identity

Trade Name
MEDIGLIDE EUDAMED
Device Name
HYPODERMIC NEEDLE EUDAMED
Model / Reference
SS-6092 EUDAMED

Identifiers

Primary DI / UDI-DI
08907265030396 EUDAMED
Basic UDI-DI
8907265N0012Z EUDAMED
EMDN Code
A0101010102 HYPODERMIC SYRINGE NEEDLES, W/O SAFETY SYSTEMS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Austria 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

Mediglide by Romsons Group Private Limited — 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
IN-MF-000036506
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 00020ac1-b19a-4351-ac2b-57f844b1db0f 61 fields · synced Jul 30, 2026