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Curette

EUDAMED

Class I (EU MDR)

Ref N/AModel UBE-D-GCZA-xxxx、UBE-FD-GCZA-xxxx、UBE-FD-GCWA-xxxx、UBE-FD-GCWB-xxxx

by Jiangsu Bonss Medical Technology Co Ltd

Identity

Device Name
Curette EUDAMED
Model / Reference
UBE-D-GCZA-xxxx、UBE-FD-GCZA-xxxx、UBE-FD-GCWA-xxxx、UBE-FD-GCWB-xxxx EUDAMED
N/A EUDAMED

Identifiers

Primary DI / UDI-DI
06942455437809 EUDAMED
Basic UDI-DI
69271553BONSS17677 EUDAMED
Direct Marketing DI
06942455437809 EUDAMED
EMDN Code
L0901 ORTHOPAEDIC SURGERY SPOONS AND CURETTES, 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: Bone curette, reusable

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

Similar devices

Also classified as Bone curette, 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 dbbaf6ae-b43e-4000-be19-d9e9da7c6bfb 61 fields · synced Jun 19, 2026