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Ambu aScope™4 Broncho - Indonesia BPOM Medical Device Registration

Ambu aScope™4 Broncho is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20703122311. The device is manufactured by AMBU A/S from Denmark, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. 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 Broncho
Analysis ID: AKL 20703122311

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

AMBU A/S

Country of Origin

Denmark

Authorized Representative

PT. AMI MEDIKA INDONESIA

AR Address

The Savoy B1-30, Jakarta Garden City Boulevard

Registration Date

Mar 06, 2023

Expiry Date

Sep 30, 2025

Product Type

Ear, Nose and Throat Surgical Equipment

Bronchoscope (flexible or rigid) and accessories.

Non Radiation Electromedics

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