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.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
AMBU SDN. BHDCountry of Origin
Malaysia
Authorized Representative
AMI MEDIKA INDONESIAAR 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

