Bone Probe

by Jiangsu Bonss Medical Technology Co Ltd 5 variants

Model UBE-D-GTZA-1001、UBE-FD-GTZA-1002、UBE-FD-GTZA-1003、UBE-FD-GTZA-1004、UBE-FD-GTZA-1005

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number69271553BONSS17473 Basic UDI-DI 06942455437960UDI-DI	Date13 Apr 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Withdrawn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

Device Name: Bone Probe
Model / Reference: UBE-D-GTZA-1001、UBE-FD-GTZA-1002、UBE-FD-GTZA-1003、UBE-FD-GTZA-1004、UBE-FD-GTZA-1005

Primary DI / UDI-DI: 06942455437960
Basic UDI-DI: 69271553BONSS17473
Direct Marketing DI: 06942455437960
EMDN Code: L0916 Orthopaedic surgery burs and tips, reusable

Device Class: Class I
EU market of registration: Austria

Manufacturer details

EUDAMED SRN: CN-MF-000023743
Authorised representative: Obelis s.a. BE-AR-000000106

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Properties

Reusable

Other properties (12)

Sterile: No
Implantable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No