APEX Domus 3 Pump and Mattress - Indonesia BPOM Medical Device Registration
APEX Domus 3 Pump and Mattress is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902513229. The device is manufactured by APEX MEDICAL (KUN SAN) CORP. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PROTECHMA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
APEX MEDICAL (KUN SAN) CORP.Country of Origin
China
Authorized Representative
PT. PROTECHMA INDONESIAAR Address
Jl. Teuku Umar KM 45,5 No.89 Cibitung Bekasi, Jawa Barat Telp : 021-88326735 Fax : 021-88328007
Registration Date
May 07, 2019
Expiry Date
Mar 01, 2024
Product Type
Therapeutic General and Individual Hospital Equipment
Alternating pressure air flotation mattress.
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