Pure Global

MANDALAI Lens - Indonesia BPOM Medical Device Registration

MANDALAI Lens is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11204810740. The device is manufactured by JIANGSU XUZHI OPTICAL GLASSES CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MUSIM MAS PARTNERS.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : A
MANDALAI Lens
Analysis ID: AKL 11204810740

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. MUSIM MAS PARTNERS

AR Address

Jl. KH. Zainul Arifin Blok B3 No. 15 Rt. 001/007 Krukut, Taman Sari

Registration Date

Sep 01, 2022

Expiry Date

Sep 01, 2025

Product Type

Therapeutic Eye Equipment

Prescription show lens.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing