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UDI Compass
Unknown / Not in EUDAMED

Snapshot 2026-10-12 · Link to EUDAMED

AlCath Flutter Black LT G

UDI-DI 04251883700488Basic UDI-DI 426009092BUDI00001F8

Class III · MDR · VascoMed GmbH

Identification
Model
—
Issuing agency
GS1
Device status
active
Sterile
Yes
Implantable
No
Measuring function
No
Reusable surgical
No
Certificates

20374GB450260819

EU technical documentation assessment · unknown

Notified body: DNV MEDCERT GmbH (0482)

Valid from 2026-08-19 · Expiry 2030-12-21

Scope not stated in certificate data.

Certificate’s own scope text — not a compliance opinion from UDI Compass.

Manufacturer

VascoMed GmbH

SRN DE-MF-000005571

DE · Binzen

manufacturer

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Showing 12 of 21 other UDI-DIs.

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Canonical device page: /device/alcath-flutter-black-lt-g-0488 · UDI page: /udi/04251883700488

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