Pure Global

ACRYSOF Multi Piece Intraocular Lens - Indonesia BPOM Medical Device Registration

ACRYSOF Multi Piece Intraocular Lens is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31202112652. The device is manufactured by ALCON RESEARCH LLC from United States, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. BINASUKSES CANTEEN.

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 : D
ACRYSOF Multi Piece Intraocular Lens
Analysis ID: AKL 31202112652

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

ALCON RESEARCH LLC

Country of Origin

United States

Authorized Representative

PT. BINASUKSES CANTEEN

AR Address

JL. PULO KAMBING II NO.26 KAWASAN INDUSTRI PULOGADUNG

Registration Date

Nov 26, 2020

Expiry Date

Jul 12, 2024

Product Type

Prosthetic Eye Equipment

Intraocular lens.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing