3M COMPLY Bowie-Dick Plus Type Test Pack - Indonesia BPOM Medical Device Registration
3M COMPLY Bowie-Dick Plus Type Test Pack is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20901420174. The device is manufactured by 3M COMPANY from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BRIDGE TWO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
3M COMPANYCountry of Origin
United States
Authorized Representative
PT. BRIDGE TWOAR Address
Jl. Petojo Melintang No. 17
Registration Date
Oct 07, 2024
Expiry Date
Mar 22, 2029
Product Type
General and Individual Hospital Equipment Monitoring
Sterilization process indicator.
Non Electromedic Non Sterile
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