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i-Optik Auto Ref/keratometer - Indonesia BPOM Medical Device Registration

i-Optik Auto Ref/keratometer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201220167. 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 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 Auto Ref/keratometer
Analysis ID: AKL 11201220167

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

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

Oct 10, 2022

Expiry Date

Feb 14, 2027

Product Type

Diagnostic Eye Equipment

Keratoscope

Non Radiation Electromedics

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