MICROLIFE Nebulizer - Indonesia BPOM Medical Device Registration
MICROLIFE Nebulizer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403520002. The device is manufactured by GLOBALCARE MEDICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. CEKINDO BUSINESS INTERNATIONAL.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GLOBALCARE MEDICAL TECHNOLOGY CO., LTD.Country of Origin
China
Authorized Representative
PT. CEKINDO BUSINESS INTERNATIONALAR Address
Gedung Axa Tower Lantai 36, Jalan Profesor Doktor Satrio Kaveling 18
Registration Date
Jan 02, 2025
Expiry Date
Sep 26, 2029
Product Type
Therapeutic Anesthesia Equipment
Nebulizer.
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