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Bone Probe

EUDAMED

Class I (EU MDR)

Ref N/AModel UBE-D-GTZA-1001、UBE-FD-GTZA-1002、UBE-FD-GTZA-1003、UBE-FD-GTZA-1004、UBE-FD-GTZA-1005

by Jiangsu Bonss Medical Technology Co Ltd

Identity

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

Identifiers

Primary DI / UDI-DI
06942455437939 EUDAMED
Basic UDI-DI
69271553BONSS17473 EUDAMED
Direct Marketing DI
06942455437939 EUDAMED
EMDN Code
L0916 ORTHOPAEDIC SURGERY BURS AND TIPS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Fluted surgical drill bit, reusable

Bone Probe by Jiangsu Bonss Medical Technology Co., Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Fluted surgical drill bit, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

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

Sources (1)

  • EUDAMED 14d18489-8edc-41c6-b70b-3e157327dcca 61 fields · synced Jun 19, 2026