FOCCUS Foculime - Indonesia BPOM Medical Device Registration
FOCCUS Foculime is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403420717. The device is manufactured by SHANGHAI NAHUI DRYING REAGENT FACTORY from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ALKESMED MAIN PARTNERS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHANGHAI NAHUI DRYING REAGENT FACTORYCountry of Origin
China
Authorized Representative
ALKESMED MAIN PARTNERSAR Address
Jl. Supriyadi No. 4B RT 03 / RW 1
Registration Date
Oct 24, 2024
Expiry Date
Oct 23, 2027
Product Type
Therapeutic Anesthesia Equipment
Carbon dioxide absorbent.
Non Electromedic Non Sterile

