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CK ARTHROPLASTY Knee Prostesis System - Indonesia BPOM Medical Device Registration

CK ARTHROPLASTY Knee Prostesis System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302420479. The device is manufactured by BEIJING CHUNLIZHENGDA MEDICAL INSTRUMENTS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ADDI SON MEDICA.

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Risk Class Kelas Resiko : C
CK ARTHROPLASTY Knee Prostesis System
Analysis ID: AKL 21302420479

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. ADDI SON MEDICA

AR Address

Jalan Ambengan No. 37, RT.010 RW.009

Registration Date

Dec 23, 2024

Expiry Date

Dec 20, 2027

Product Type

Prosthetic Orthopedic Equipment

Knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis.

Non Electromedic Sterile

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