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UDI Compass

Tornier Perform® Reversed Glenoid

Unknown / Not in EUDAMED

Snapshot 2026-10-31 · Link to EUDAMED

UDI-DI 00846832092116Basic UDI-DI 08858251006542TP

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Class III · MDR · Tornier, Inc.

Identification

Model
08858251006542TP
Issuing agency
GS1
Device status
active
Sterile
Yes
Implantable
Yes
Measuring function
No
Reusable surgical
No

Certificates

MDR 730968

EU technical documentation assessment · unknown

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

Valid from 2025-11-04 · Expiry 2028-11-28

Scope not stated in certificate data.

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

Manufacturer

Tornier, Inc.

SRN US-MF-000025261

US · Minnesota

manufacturer

Authorised representative: Stryker European Operations Limited (IE-AR-000000092)

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NameUDI-DICertificate
Tornier Perform® Reversed Augmented Glenoid00846832092079
Unknown / Not in EUDAMED

Snapshot 2026-10-31 · Link to EUDAMED

Tornier Perform® Reversed Augmented Glenoid00846832092093
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Tornier Perform® Reversed Augmented Glenoid00846832092123
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Tornier Perform® Reversed Augmented Glenoid00846832092109
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Tornier Perform® Reversed Augmented Glenoid00846832092130
Unknown / Not in EUDAMED

Snapshot 2026-10-31 · Link to EUDAMED

Tornier Perform® Reversed Augmented Glenoid00846832092154
Unknown / Not in EUDAMED

Snapshot 2026-10-31 · Link to EUDAMED

Tornier Perform® Reversed Augmented Glenoid00846832092147
Unknown / Not in EUDAMED

Snapshot 2026-10-31 · Link to EUDAMED

Tornier Perform® Reversed Augmented Glenoid00846832092086
Unknown / Not in EUDAMED

Snapshot 2026-10-31 · Link to EUDAMED

Tornier Perform® Reversed Glenoid00846832092161
Unknown / Not in EUDAMED

Snapshot 2026-10-31 · Link to EUDAMED

All UDI-DIs in this Basic UDI-DI family

Canonical device page: /device/tornier-perform-reversed-glenoid-2116 · UDI page: /udi/00846832092116

All devices from Tornier, Inc.