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ESSILOR Refraction - Indonesia BPOM Medical Device Registration

ESSILOR Refraction is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10102911272. The device is manufactured by YURATEK ELEKTRONIK VE TIBBI CIHAZLAR LTD., STI. from Turkey, 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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BPOM Registered
Risk Class Kelas Resiko : A
ESSILOR Refraction
Analysis ID: AKL 10102911272

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Turkey

Authorized Representative

PT. OPTICAL PARTNERS INDONESIA

AR Address

JL. TOMANG RAYA NO 15A, TOMANG GROGOL PETAMBURAN

Registration Date

Aug 12, 2022

Expiry Date

Aug 31, 2025

Product Type

Clinical Laboratory Equipment

Refractometer for clinical use. (Electrically Operated)

Non Radiation Electromedics

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