Bonss

by Jiangsu Bonss Medical Technology Co Ltd 51 variants

Model ES-HD1、ES-HD2、ES-4K1、ES-4K2、TS-HD1、TS-HD2、LS-HD1、LS-HD2、ETS-HD1、ETS-HD2

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, self-declared

Class I: no certifier involved

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	Number69271553BONSS0406D Basic UDI-DI 06927155320019UDI-DI	Date16 Dec 2022Registered	StatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name: Endoscopic Camera System
Model / Reference: ES-HD1、ES-HD2、ES-4K1、ES-4K2、TS-HD1、TS-HD2、LS-HD1、LS-HD2、ETS-HD1、ETS-HD2

Primary DI / UDI-DI: 06927155320019
Basic UDI-DI: 69271553BONSS0406D
Direct Marketing DI: 06927155320019
EMDN Code: Z12020402 Light sources for endoscopy and minimally invasive surgery

Device Class: Class I
EU market of registration: Austria

Manufacturer details

EUDAMED SRN: CN-MF-000023743
Authorised representative: Sungo Cert GmbH DE-AR-000010869

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Properties

Other properties (13)

Sterile: No
Implantable: No
Reusable: 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