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80430

EUDAMED

Class IIa (EU MDR)

Ref 80430Model ENDOKIT

by Advance Medical Integration Systems

Identity

Trade Name
80430 EUDAMED
Device Name
80430 EUDAMED
Model / Reference
ENDOKIT EUDAMED
80430 EUDAMED

Identifiers

Primary DI / UDI-DI
03770013585272 EUDAMED
Basic UDI-DI
B-03770013585272 EUDAMED
EMDN Code
G0380 DIGESTIVE ENDOSCOPY DEVICES - ACCESSORIES 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

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

80430 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 f11b2c43-44af-4c8a-80a5-8b707422e2c5 61 fields · synced Jun 17, 2026