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UDI Compass

PROCEED

Unknown / Not in EUDAMED

Snapshot 2026-11-02 · Link to EUDAMED

UDI-DI 10705031047785Basic UDI-DI 0705031a011534J

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Class III · MDR · Johnson & Johnson International

Identification

Model
PROCEED Surgical Mesh
Issuing agency
GS1
Device status
active
Sterile
Yes
Implantable
Yes
Measuring function
No
Reusable surgical
No

Certificates

MDR 730258

EU technical documentation assessment · unknown

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

Valid from 2026-09-10 · Expiry 2031-01-04

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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NameUDI-DICertificate
PROCEED10705031047792
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PROCEED10705031047716
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PROCEED10705031047778
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PROCEED10705031047723
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PROCEED10705031047730
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PROCEED10705031047747
Unknown / Not in EUDAMED

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PROCEED10705031047693
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PROCEED10705031047709
Unknown / Not in EUDAMED

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PROCEED10705031047761
Unknown / Not in EUDAMED

Snapshot 2026-11-02 · Link to EUDAMED

PROCEED10705031047754
Unknown / Not in EUDAMED

Snapshot 2026-11-02 · Link to EUDAMED

All UDI-DIs in this Basic UDI-DI family

Canonical device page: /device/proceed-7785 · UDI page: /udi/10705031047785

All devices from Johnson & Johnson International