POLYFUSION Infusion Set - Indonesia BPOM Medical Device Registration
POLYFUSION Infusion Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902603225. The device is manufactured by POLY MEDICURE LIMITED from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEGAH MEDIKA PHARMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
POLY MEDICURE LIMITEDCountry of Origin
India
Authorized Representative
PT. MEGAH MEDIKA PHARMAAR Address
Jl. Minangkabau Timur Raya No. 07 RT 006 RW 008
Registration Date
Oct 03, 2024
Expiry Date
Mar 31, 2029
Product Type
Therapeutic General and Individual Hospital Equipment
Intravascular administration set
Non Electromedic Sterile
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