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UDI Compass

Pro-AB Mesh

Certificate valid

Snapshot 2026-11-02 · Link to EUDAMED

UDI-DI 08904248251090Basic UDI-DI 89042482PRB012M7

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Class III · MDR · TI Medical Private Limited

Identification

Model
Poly (Glycolide co-caprolactone) and Polypropylene Mesh
Issuing agency
GS1
Device status
active
Sterile
Yes
Implantable
Yes
Measuring function
No
Reusable surgical
No

Certificates

2975-MED-2608201-D01

EU technical documentation assessment · valid

Notified body: SZUTEST Konformitätsbewertungsstelle GmbH (2975)

Valid from 2026-03-23 · Expiry 2031-03-22

Scope not stated in certificate data.

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

2975-MED-2608201

EU quality management system · valid

Notified body: SZUTEST Konformitätsbewertungsstelle GmbH (2975)

Valid from 2026-03-23 · Expiry 2031-03-22

Scope not stated in certificate data.

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

Manufacturer

TI Medical Private Limited

SRN IN-MF-000026561

IN · Dehradun

manufacturer

Authorised representative: Obelis s.a. (BE-AR-000000106)

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Showing 12 of 21 other UDI-DIs.

All UDI-DIs in this Basic UDI-DI family

Canonical device page: /device/pro-ab-mesh-1090 · UDI page: /udi/08904248251090

All devices from TI Medical Private Limited