Fenestrated polyax. pedicle screw 9x50, dual-diam

by Medacta International SA

Ref 03.60.373Model Spine MUST screw (tulip)

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number764014274VIS0084R061YS Basic UDI-DI 07630030861949UDI-DI	Date28 May 2026Registered	StatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference: Spine MUST screw (tulip), 03.60.373

Primary DI / UDI-DI: 07630030861949
Basic UDI-DI: 764014274VIS0084R061YS
EMDN Code: P09070302 Thoracolumbosacral fixation systems

Device Class: Class IIb
EU market of registration: Italy

Manufacturer details

EUDAMED SRN: CH-MF-000033473
Authorised representative: Medacta Italia srl IT-AR-000022505

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Properties

Sterile
Implantable
Sutures
CMR Substance

Other properties (10)

Reusable: No
Contains Latex: No
Reprocessed: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No