FOCCUS Guedel Airway - Indonesia BPOM Medical Device Registration
FOCCUS Guedel Airway is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403520114. The device is manufactured by BONREE MEDICAL CO., LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ALKESMED MAIN PARTNERS.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
BONREE MEDICAL CO., LTDCountry of Origin
China
Authorized Representative
PT. ALKESMED MAIN PARTNERSAR Address
Jl. Supriyadi No. 4B RT 03 / RW 1
Registration Date
Feb 03, 2025
Expiry Date
Feb 03, 2028
Product Type
Therapeutic Anesthesia Equipment
Oropharyngeal airway
Non Electromedic Sterile
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