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ARTIBEST Intra-articular Injection - Indonesia BPOM Medical Device Registration

ARTIBEST Intra-articular Injection is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31302220196. The device is manufactured by MAXIGEN BIOTECH INC. from Taiwan (China), and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. QUALTEK CONSULTANT JAKARTA.

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 : D
ARTIBEST Intra-articular Injection
Analysis ID: AKL 31302220196

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Taiwan (China)

Authorized Representative

PT. QUALTEK CONSULTANT JAKARTA

AR Address

Icon Business Park Blok K No 6, BSD City, Kab Tangerang, Banten

Registration Date

Apr 27, 2022

Expiry Date

Nov 30, 2026

Product Type

Prosthetic Orthopedic Equipment

Intra articular fluid

Non Electromedic Sterile

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