DECONEX ENDOMATIC - Indonesia BPOM Medical Device Registration
DECONEX ENDOMATIC is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903717683. 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
Jul 25, 2022
Expiry Date
May 10, 2024
Product Type
General Hospital Equipment and Other Individuals
Liquid chemical sterilants/high level disinfectants.
Non Electromedic Non Sterile
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DECONEX Foam Active
DECONEX 64 Neutradry
Deconex Foam Plus
DECONEX Prozyme Active
DECONEX 34 GR Acidic Special Detergent
OPTIMUM Sterilization Flat Reel
JIANGSU PAKION MEDICAL MATERIAL CO., LTD
OPTIMUM Sterilization Packaging Crepe Paper
JIANGSU PAKION MEDICAL MATERIAL CO., LTD
FULCARE Rapid Readout Biological Indicator for EtO
CHENGDU FULCARE TRADING CO., LTD
Actosed PA Powder
GMBH ACT
DECONEX Solarsept
BORER CHEMIE AG.
Deconex Lube Spray
BORER CHEMIE AG.
Indicator Tape with EO indicator
GKE-GMBH.
DECONEX 34 GR
BORER CHEMIE AG.
DECONEX Instrument Plus
BORER CHEMIE AG
Deconex Foam Plus
BORER CHEMIE AG.