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A.M.I Wi-3 HAL-RAR System - Indonesia BPOM Medical Device Registration

A.M.I Wi-3 HAL-RAR System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20804513370. The device is manufactured by A.M.I AGENCY FOR MEDICAL INNOVATIONS GMBH. from Austria, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is DIAN LANGGENG PRATAMA.

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 : B
A.M.I Wi-3 HAL-RAR System
Analysis ID: AKL 20804513370

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Austria

Authorized Representative

DIAN LANGGENG PRATAMA

AR Address

Gedung Dinar, Jl. Raden Saleh Raya No. 4 RT.10/RW.01, Kel. Kenari, Kec. Senen. Kota Adm. Jakarta Pusat, Provinsi DKI Jakarta, Kode Pos 10430

Registration Date

Apr 18, 2023

Expiry Date

Dec 31, 2026

Product Type

Gastroenterology-Surgical Urology Equipment

Hemorrhoidal ligator.

Non Radiation Electromedics

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