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50390

EUDAMED

Class IIa (EU MDR)

Ref 50390Model ENDOPUMP

by Advance Medical Integration Systems

Identity

Trade Name
50390 EUDAMED
Device Name
50390 EUDAMED
Model / Reference
ENDOPUMP EUDAMED
50390 EUDAMED

Identifiers

Primary DI / UDI-DI
03770013585548 EUDAMED
Basic UDI-DI
B-03770013585548 EUDAMED
EMDN Code
G0380 DIGESTIVE ENDOSCOPY DEVICES - ACCESSORIES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

No

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: Gastro-urological guidewire, single-use

50390 by Advance Medical Integration Systems — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Gastro-urological guidewire, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
FR-MF-000014717

Sources (1)

  • EUDAMED 938e36ea-2a11-4703-b9c0-a4d203ba2a53 61 fields · synced Jul 21, 2026