FRESCO Infusion Set Vented - Indonesia BPOM Medical Device Registration
FRESCO Infusion Set Vented is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902220819. The device is manufactured by ROMSONS INTERNATIONAL (UNIT II) from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ABADINUSA USAHASEMESTA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ROMSONS INTERNATIONAL (UNIT II)Country of Origin
India
Authorized Representative
PT. ABADINUSA USAHASEMESTAAR Address
Jalan Raden Saleh No. 45 G
Registration Date
Jul 28, 2022
Expiry Date
Jul 28, 2025
Product Type
Therapeutic General and Individual Hospital Equipment
Intravascular administration set
Non Electromedic Sterile
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