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Solojekt Ad

EUDAMED

Class IIa (EU MDR)

Ref IT-02-23-LLModel SOLOJEKT AD

by I'M Medicare SARL

Identity

Trade Name
SOLOJEKT AD EUDAMED
Device Name
AD/RUP SYRINGE WITH NEEDLE EUDAMED
Model / Reference
SOLOJEKT AD EUDAMED
IT-02-23-LL EUDAMED

Identifiers

Primary DI / UDI-DI
06118002220242 EUDAMED
Basic UDI-DI
611800222ADRUPVZ EUDAMED
EMDN Code
A020199 SYRINGES, SINGLE-USE - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
France 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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Solojekt Ad by I'M Medicare SARL — 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

Manufacturer
I'M Medicare SARL
EUDAMED SRN
MA-MF-000037665
Authorised Representative
EUCEREP B.V. NL-AR-000001966

Sources (1)

  • EUDAMED 177a6b5e-daa5-4185-8819-42c25905b2a7 61 fields · synced Jun 18, 2026