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CATAPULSE Lens Removal System - Indonesia BPOM Medical Device Registration

CATAPULSE Lens Removal System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203220179. The device is manufactured by MED-LOGICS INC from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. HARLISA TRUE GRACE.

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
CATAPULSE Lens Removal System
Analysis ID: AKL 21203220179

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

MED-LOGICS INC

Country of Origin

United States

Authorized Representative

PT. HARLISA TRUE GRACE

AR Address

Perum Sedati Permai Jl. Sriti HH-15

Registration Date

Dec 12, 2022

Expiry Date

Aug 15, 2027

Product Type

Surgical Eye Equipment

Phacofragmentation system.

Non Radiation Electromedics

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