← Back to catalogue

Punch

EUDAMED

Class I (EU MDR)

Ref N/AModel UBE-C-HXYA-xxxx、UBE-C-HXYB-xxxx、UBE-FD-YGQP-xxxx、UBE-FD-YGQH-xxxx、UBE-FD-YGQT-xxxx、UBE-FD-YGTH-xxxx、UBE-FD-YGTS-0000、UBE-FD-YGQF-xxxx

by Jiangsu Bonss Medical Technology Co Ltd

Identity

Device Name
Punch EUDAMED
Model / Reference
UBE-C-HXYA-xxxx、UBE-C-HXYB-xxxx、UBE-FD-YGQP-xxxx、UBE-FD-YGQH-xxxx、UBE-FD-YGQT-xxxx、UBE-FD-YGTH-xxxx、UBE-FD-YGTS-0000、UBE-FD-YGQF-xxxx EUDAMED
N/A EUDAMED

Identifiers

Primary DI / UDI-DI
06942455435898 EUDAMED
Basic UDI-DI
69271553BONSS1706T EUDAMED
Direct Marketing DI
06942455435898 EUDAMED
EMDN Code
L091303 BONE REDUCTION FORCEPS, 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

Punch 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED 3e93e1eb-6261-4bb6-a34a-3deb83f7868e 61 fields · synced Jun 18, 2026