APEX Alternating Pressure Relief System - Indonesia BPOM Medical Device Registration
APEX Alternating Pressure Relief System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902420399. The device is manufactured by APEX MEDICAL CORP. from Taiwan (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 CORP.Country of Origin
Taiwan (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
Apr 23, 2024
Expiry Date
Aug 24, 2028
Product Type
Therapeutic General and Individual Hospital Equipment
Alternating pressure air flotation mattress.
Non Radiation Electromedics
