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UDI Compass

Vanta™ AdaptiveStim™

Certificate valid

Snapshot 2026-11-02 · Link to EUDAMED

UDI-DI 00763000947620Basic UDI-DI 0199309B0000029K9

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Class III · MDR · Medtronic, Inc.

Identification

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

Certificates

G70 039709 1363

EU technical documentation assessment · valid

Notified body: TÜV SÜD Product Service GmbH (0123)

Valid from 2026-09-02 · Expiry 2031-09-01

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)

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Vanta™ AdaptiveStim™00763000947637
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Vanta™ AdaptiveStim™00763000947590
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Vanta™ AdaptiveStim™00763000968366
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Vanta™ AdaptiveStim™00763000968373
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Vanta™ AdaptiveStim™00763000968380
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Snapshot 2026-11-02 · Link to EUDAMED

All UDI-DIs in this Basic UDI-DI family

Canonical device page: /device/vantatm-adaptivestimtm-7620 · UDI page: /udi/00763000947620

All devices from Medtronic, Inc.