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Balloon Kyphoplasty Kits

EUDAMED

Class IIa (EU MDR)

Ref A500325Model K02D

by Beijing Bonsci Technology Co., Ltd.

Identity

Device Name
Balloon Kyphoplasty Kits EUDAMED
Model / Reference
K02D EUDAMED
A500325 EUDAMED

Identifiers

Primary DI / UDI-DI
06974754671233 EUDAMED
Basic UDI-DI
B-06974754671233 EUDAMED
EMDN Code
P091399 ORTHOPAEDIC IMPLANT INSTRUMENTS, SINGLE-USE - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Joint prosthesis implantation kit, single-use

Balloon Kyphoplasty Kits by Beijing Bonsci Technology Co., Ltd. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Joint prosthesis implantation kit, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
CN-MF-000013535
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED dbe78352-7eb5-487a-a714-54ffc56ad15e 61 fields · synced Jun 19, 2026