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UDI Compass
Unknown / Not in EUDAMED

Snapshot 2026-10-13 · Link to EUDAMED

MYNXGRIP™ Vascular Closure Device 5F

UDI-DI 10862028000403Basic UDI-DI 07050320000000000000040CD

Class III · MDR · Cordis US Corp.

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

MDR 771921

EU technical documentation assessment · unknown

Notified body: BSI Group The Netherlands B.V. (2797)

Valid from 2026-06-11 · Expiry 2029-04-22

Scope not stated in certificate data.

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

Manufacturer

Cordis US Corp.

SRN US-MF-000020031

US · Miami Lakes

manufacturer

Authorised representative: Cordis Cashel (IE-AR-000017793)

Related UDI-DIs

All UDI-DIs in this Basic UDI-DI family

Canonical device page: /device/mynxgriptm-vascular-closure-device-5f-0403 · UDI page: /udi/10862028000403

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