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Burs

EUDAMED

Class IIa (EU MDR)

Ref N/AModel DGA、DGB、DGC、DGD、DGE

by Jiangsu Bonss Medical Technology Co Ltd

Identity

Device Name
Burs EUDAMED
Model / Reference
DGA、DGB、DGC、DGD、DGE EUDAMED
N/A EUDAMED

Identifiers

Primary DI / UDI-DI
06942455418006 EUDAMED
Basic UDI-DI
69271553BONSS2516U EUDAMED
EMDN Code
Z12010985 ELECTROSURGERY INSTRUMENTS - CONSUMABLES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Ireland EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

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: Endoscopic electrosurgical handpiece/electrode, bipolar, single-use

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

Similar devices

Also classified as Endoscopic electrosurgical handpiece/electrode, bipolar, single-use.

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 7a77dfb4-939d-4f40-8191-70837b453961 61 fields · synced Jun 17, 2026