HD Vented Spike Infusion Administration Set - Indonesia BPOM Medical Device Registration
HD Vented Spike Infusion Administration Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902113180. The device is manufactured by JIANGXI HONGDA MEDICAL EQUIPMENT GROUP LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is MIRACHEN INACI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
JIANGXI HONGDA MEDICAL EQUIPMENT GROUP LTDCountry of Origin
China
Authorized Representative
MIRACHEN INACIAR Address
Jl. Mayor Pol. Zainal Arifin No. 159A, RT.59, Kelurahan Sumber Rejo, Kecamatan Balikpapan Tengah, Kota Balikpapan, Prov. Kalimantan Timur
Registration Date
Mar 06, 2024
Expiry Date
Feb 20, 2029
Product Type
Therapeutic General and Individual Hospital Equipment
Intravascular administration set
Non Electromedic Sterile
