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AMO Intralase Advance Femto Second Laser System - Indonesia BPOM Medical Device Registration

AMO Intralase Advance Femto Second Laser System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203212813. The device is manufactured by AMO MANUFACTURING USA LLC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEDIUM FIRST.

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
AMO Intralase Advance Femto Second Laser System
Analysis ID: AKL 21203212813

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. MEDIUM FIRST

AR Address

The Belleza Permata Hijau GP Office Tower Lt. 27, Jl. Letjen Soepeno No. 34

Registration Date

Dec 14, 2023

Expiry Date

Sep 08, 2027

Product Type

Surgical Eye Equipment

Ophthalmic laser.

Non Radiation Electromedics

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