Pure Global

HOYALUX iD MySelf - Indonesia BPOM Medical Device Registration

HOYALUX iD MySelf is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11204220445. The device is manufactured by HOYA LENS THAILAND LIMITED from Thailand, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. HOYA LENS 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : A
HOYALUX iD MySelf
Analysis ID: AKL 11204220445

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Thailand

Authorized Representative

PT. HOYA LENS INDONESIA

AR Address

Wisma Lumbini , Lt3 , Jl Tomang Raya no:53 , Tomang ,Jakarta barat 11440

Registration Date

Dec 13, 2022

Expiry Date

Apr 12, 2027

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