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ESSILOR Pupillometer - Indonesia BPOM Medical Device Registration

ESSILOR Pupillometer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201913821. The device is manufactured by ESSILOR INSTRUMENTS, A DIVISION OF ESSILOR INTERNATIONAL 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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BPOM Registered
Risk Class Kelas Resiko : A
ESSILOR Pupillometer
Analysis ID: AKL 11201913821

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

France

Authorized Representative

PT. OPTICAL PARTNERS INDONESIA

AR Address

JL. TOMANG RAYA NO 15A, TOMANG GROGOL PETAMBURAN

Registration Date

Feb 05, 2024

Expiry Date

Jan 31, 2028

Product Type

Diagnostic Eye Equipment

Pupillometer.

Non Radiation Electromedics

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