Deconex Foam Plus - Indonesia BPOM Medical Device Registration
Deconex Foam Plus is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903420314. The device is manufactured by BORER CHEMIE AG. from Switzerland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is FIVE ALIGNED DISPOS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BORER CHEMIE AG.Country of Origin
Switzerland
Authorized Representative
FIVE ALIGNED DISPOSAR Address
Jl. Pulo Sirih Barat Blok M/15, Jaka Setia, Bekasi 17147
Registration Date
Apr 05, 2024
Expiry Date
Mar 24, 2027
Product Type
General Hospital Equipment and Other Individuals
Liquid chemical sterilants/high level disinfectants.
Non Electromedic Non Sterile
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