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Nucleus Pulposus Forceps

EUDAMED

Class I (EU MDR)

Ref N/AModel UBE-C-SHZA-xxxx、UBE-C-SHZB-xxxx、UBE-C-SHWA-xxxx、UBE-C-SHWB-xxxx、UBE-C-KTSA-xxxx、UBE-FD-SHQZ-xxxx、UBE-FD-SHQW-xxxx、UBE-FD-SHZA-xxxx、UBE-FD-SHYZ-xxxx、UBE-FD-SHWA-xxxx、UBE-FD-SHYW-xxxx、UBE-FD-SHMZ-xxxx、UBE-FD-SHMW-xxxx

by Jiangsu Bonss Medical Technology Co Ltd

Identity

Device Name
Nucleus Pulposus Forceps EUDAMED
Model / Reference
UBE-C-SHZA-xxxx、UBE-C-SHZB-xxxx、UBE-C-SHWA-xxxx、UBE-C-SHWB-xxxx、UBE-C-KTSA-xxxx、UBE-FD-SHQZ-xxxx、UBE-FD-SHQW-xxxx、UBE-FD-SHZA-xxxx、UBE-FD-SHYZ-xxxx、UBE-FD-SHWA-xxxx、UBE-FD-SHYW-xxxx、UBE-FD-SHMZ-xxxx、UBE-FD-SHMW-xxxx EUDAMED
N/A EUDAMED

Identifiers

Primary DI / UDI-DI
06942455437229 EUDAMED
Basic UDI-DI
69271553BONSS1716V EUDAMED
Direct Marketing DI
06942455437229 EUDAMED
EMDN Code
L091399 ORTHOPAEDIC SURGERY FORCEPS, REUSABLE - OTHER 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

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

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Jiangsu Bonss Medical Technology Co Ltd
EUDAMED SRN
CN-MF-000023743
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED a91af5f7-2c17-4ba7-bc9a-be6311da9139 61 fields · synced Jun 18, 2026