SERENITY Alternating Pressure Pump & Mattress - Indonesia BPOM Medical Device Registration
SERENITY Alternating Pressure Pump & Mattress is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902112700. The device is manufactured by AIRFLO (XIAMEN) MEDICAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SERENITY INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
AIRFLO (XIAMEN) MEDICAL CO., LTD.Country of Origin
China
Authorized Representative
PT. SERENITY INDONESIAAR Address
Komplek Ruko Permata Kota Blok Q No. 10 Jl. Pangeran Tubagus Angke No.170 RT.010 RW . 01
Registration Date
May 29, 2023
Expiry Date
Feb 07, 2028
Product Type
Therapeutic General and Individual Hospital Equipment
Alternating pressure air flotation mattress.
Non Radiation Electromedics
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