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Capsulaser Cataract System - Indonesia BPOM Medical Device Registration

Capsulaser Cataract System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203420063. The device is manufactured by RH USA from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. KATAMATA OPTOMEDIK.

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
Capsulaser Cataract System
Analysis ID: AKL 21203420063

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

RH USA

Country of Origin

United States

Authorized Representative

PT. KATAMATA OPTOMEDIK

AR Address

Komplek Ketapang Indah Blok B2 No.31 Jl. KH. Zainul Arifin Kel.Krukut, Kec.Taman Sari Jakarta Barat

Registration Date

Mar 31, 2024

Expiry Date

Dec 31, 2025

Product Type

Surgical Eye Equipment

Ophthalmic laser.

Non Radiation Electromedics

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