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Optec Plus Vision Screener - Indonesia BPOM Medical Device Registration

Optec Plus Vision Screener is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201320343. The device is manufactured by STEREO OPTICAL COMPANY, INC from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. FA ANTARES 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
Optec Plus Vision Screener
Analysis ID: AKL 11201320343

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

United States

Authorized Representative

PT. FA ANTARES MEDIKA

AR Address

RUKO GOLDEN BOULEVARD BLOK I NO.7

Registration Date

Jul 18, 2023

Expiry Date

Jul 17, 2025

Product Type

Diagnostic Eye Equipment

Color vision tester.

Non Radiation Electromedics

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