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i-Optik Computerized Vision Tester - Indonesia BPOM Medical Device Registration

i-Optik Computerized Vision Tester is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201320366. The device is manufactured by NINGBO MING SING OPTICAL R&D CO., LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SURYA TAMA MEDIKA.

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 : A
i-Optik Computerized Vision Tester
Analysis ID: AKL 11201320366

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. SURYA TAMA MEDIKA

AR Address

Jl m hasibuan ruko suncity pbb. 37 real blok e.27 rt 004 rw 002 kel margajaya kec bekasi selatan kota bekasi

Registration Date

Sep 20, 2023

Expiry Date

Feb 14, 2027

Product Type

Diagnostic Eye Equipment

Color vision tester.

Non Radiation Electromedics

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