APEX Domus 2 Pump and Mattress - Indonesia BPOM Medical Device Registration
APEX Domus 2 Pump and Mattress is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902513225. The device is manufactured by APEX MEDICAL (KUN SHAN) CORP. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PROTECHMA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
APEX MEDICAL (KUN SHAN) CORP.Country of Origin
China
Authorized Representative
PROTECHMA INDONESIAAR Address
JL. Teuku Umar No. 89 KM. 45,5, Kode Pos 17530, Desa/Kelurahan Sukadanau, Kec. Cikarang Barat, Kab. Bekasi, Prov. Jawa Barat
Registration Date
Dec 28, 2023
Expiry Date
Aug 24, 2028
Product Type
Therapeutic General and Individual Hospital Equipment
Alternating pressure air flotation mattress.
Non Radiation Electromedics

