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Ambu aScope™ 4 Cysto - Indonesia BPOM Medical Device Registration

Ambu aScope™ 4 Cysto is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801125922. The device is manufactured by AMBU SDN. BHD from Malaysia, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is AMI MEDIKA INDONESIA.

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
Ambu aScope™ 4 Cysto
Analysis ID: AKL 20801125922

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

AMBU SDN. BHD

Country of Origin

Malaysia

Authorized Representative

AMI MEDIKA INDONESIA

AR Address

The Savoy B1-30, Jakarta Garden City Boulevard

Registration Date

Sep 22, 2021

Expiry Date

Sep 30, 2025

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories

Non Radiation Electromedics

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