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ENSILOR VISIOSMART - Indonesia BPOM Medical Device Registration

ENSILOR VISIOSMART is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201220041. The device is manufactured by ESSILOR from France, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. OPTICAL PARTNERS 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.

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Risk Class Kelas Resiko : A
ENSILOR VISIOSMART

ESSILOR VISIOSMART

Analysis ID: AKL 11201220041

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

ESSILOR

Country of Origin

France

Authorized Representative

PT. OPTICAL PARTNERS INDONESIA

AR Address

JL. TOMANG RAYA NO 15A, TOMANG GROGOL PETAMBURAN

Registration Date

Feb 21, 2022

Expiry Date

Aug 31, 2025

Product Type

Diagnostic Eye Equipment

Perimeter.

Non Radiation Electromedics

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