LAICA Ultrasonic Humidifier - Indonesia BPOM Medical Device Registration
LAICA Ultrasonic Humidifier is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403611978. The device is manufactured by LAICA S.P.A. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is INNOVATION HEALTHCARE INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LAICA S.P.A.Country of Origin
Italy
Authorized Representative
INNOVATION HEALTHCARE INDONESIAAR Address
Komplek Ruko Permata Kota, Blok Q No. 11 Jl. Pangeran Tubagus Angke No. 170 Kel. Penjagalan, Kec. Penjaringan, Jakarta Utara 14450
Registration Date
Jun 26, 2023
Expiry Date
Mar 31, 2025
Product Type
Therapeutic Anesthesia Equipment
Respiratory gas humidifier.
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