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LDK Knee Joint Prosthesis System (1) - Indonesia BPOM Medical Device Registration

LDK Knee Joint Prosthesis System (1) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302520019. The device is manufactured by BEIJING LIDAKANG TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is INTER RAYA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : C
LDK Knee Joint Prosthesis System (1)
Analysis ID: AKL 21302520019

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

INTER RAYA

AR Address

Bintaro Business Center, Jl. RC Veteran No.1-i, Pesanggrahan - Jakarta Selatan

Registration Date

Jan 17, 2025

Expiry Date

Sep 23, 2029

Product Type

Prosthetic Orthopedic Equipment

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

Non Electromedic Sterile

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