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UDI Compass

ULTRAPRO

Certificate valid

Snapshot 2026-11-02 · Link to EUDAMED

UDI-DI 10705031132467Basic UDI-DI 0705031a0000943

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Class III · MDR · Johnson & Johnson International

Identification

Model
ULTRAPRO Hernia System
Issuing agency
GS1
Device status
active
Sterile
Yes
Implantable
Yes
Measuring function
No
Reusable surgical
No

Certificates

MDR 730049

EU technical documentation assessment · valid

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

Valid from 2026-01-08 · Expiry 2031-01-07

Scope not stated in certificate data.

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

Manufacturer

Johnson & Johnson International

SRN BE-MF-000008018

BE · Diegem

manufacturer

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All UDI-DIs in this Basic UDI-DI family

Canonical device page: /device/ultrapro-2467 · UDI page: /udi/10705031132467

All devices from Johnson & Johnson International