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BONE-XB - Indonesia BPOM Medical Device Registration

BONE-XB is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602023517. The device is manufactured by MEDPARK CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BINTANG SAUDARA SEMESTA JAYA.

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
BONE-XB
Analysis ID: AKL 20602023517

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

MEDPARK CO., LTD.

Country of Origin

Korea

Authorized Representative

PT. BINTANG SAUDARA SEMESTA JAYA

AR Address

Jl.Asia No.212 A-B, Medan

Registration Date

Jun 27, 2020

Expiry Date

Dec 31, 2024

Product Type

Prosthetic Dental Equipment

Bone grafting material.

Non Electromedic Sterile

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