DreamWear Full Face Mask - Indonesia BPOM Medical Device Registration
DreamWear Full Face Mask is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403816634. The device is manufactured by RESPIRONICS MEDICAL PRODUCTS (SHENZHEN) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. PHILIPS INDONESIA COMMERCIAL.
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Risk Classification
Product Class
Kelas : 1
Country of Origin
China
Authorized Representative
PT. PHILIPS INDONESIA COMMERCIALAR Address
Gedung Cibis Nine Lantai 10, Jl. TB Simatupang No. 2
Registration Date
Apr 20, 2022
Expiry Date
Apr 15, 2026
Product Type
Therapeutic Anesthesia Equipment
Oxygen mask.
Non Electromedic Non Sterile
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