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The Reflex Neo - Indonesia BPOM Medical Device Registration

The Reflex Neo is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203420044. The device is manufactured by ELLEX MEDICAL PTY., LTD. from Australia, and is classified as Risk Class Kelas Resiko : C. 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 : C
The Reflex Neo

TANGO Reflex Neo

Analysis ID: AKL 21203420044

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Australia

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

Feb 13, 2024

Expiry Date

May 09, 2025

Product Type

Surgical Eye Equipment

Ophthalmic laser.

Non Radiation Electromedics

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