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PATHLOC-LC Lateral Cage System - Indonesia BPOM Medical Device Registration

PATHLOC-LC Lateral Cage System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302717975. The device is manufactured by L&K BIOMED CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ANDAMAN MEDICAL INDONESIA.

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
PATHLOC-LC Lateral Cage System
Analysis ID: AKL 21302717975

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

PT. ANDAMAN MEDICAL INDONESIA

AR Address

Jl. DI Panjaitan KO Cawang KIR No. 10 RT. 008/002, Cipinang Cempedak, Jatinegara, Jakarta Timur

Registration Date

Feb 18, 2019

Expiry Date

Dec 05, 2023

Product Type

Prosthetic Orthopedic Equipment

Intervertebral body fusion device

Non Electromedic Non Sterile

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