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UDI Compass

SenSight™

Unknown / Not in EUDAMED

Snapshot 2026-11-02 · Link to EUDAMED

UDI-DI 00199150032419Basic UDI-DI 0763000B00024507X

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Class III · MDR · Medtronic, Inc.

Identification

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

Certificates

G70 039709 1513

EU technical documentation assessment · unknown

Notified body: TÜV SÜD Product Service GmbH (0123)

Valid from 2026-08-10 · Expiry 2029-12-16

Scope not stated in certificate data.

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

Manufacturer

Medtronic, Inc.

SRN US-MF-000019977

US · Minneapolis

manufacturer

Authorised representative: Medtronic B.V. (NL-AR-000006050)

Related UDI-DIs

NameUDI-DICertificate
SenSight™00199150032402
Unknown / Not in EUDAMED

Snapshot 2026-11-02 · Link to EUDAMED

SenSight™00199150032433
Unknown / Not in EUDAMED

Snapshot 2026-11-02 · Link to EUDAMED

SenSight™00199150032426
Unknown / Not in EUDAMED

Snapshot 2026-11-02 · Link to EUDAMED

All UDI-DIs in this Basic UDI-DI family

Canonical device page: /device/sensighttm-2419 · UDI page: /udi/00199150032419

All devices from Medtronic, Inc.