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.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
AMBU A/SCountry of Origin
Denmark
Authorized Representative
PT. AMI MEDIKA INDONESIAAR 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.
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