NEMOTO Pressure Tube - Indonesia BPOM Medical Device Registration
NEMOTO Pressure Tube is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902124513. The device is manufactured by PASIFIC HOSPITAL SUPPLY CO., LTD. from Taiwan (China), and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is INTIMEDIKA PUSPA INDAH.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
PASIFIC HOSPITAL SUPPLY CO., LTD.Country of Origin
Taiwan (China)
Authorized Representative
INTIMEDIKA PUSPA INDAHAR Address
Jl. Boulevard Raya Blok QJ 7/9 Kelapa Gading Permai - Jakarta
Registration Date
Aug 02, 2023
Expiry Date
Dec 31, 2026
Product Type
Therapeutic General and Individual Hospital Equipment
Intravascular administration set
Non Electromedic Sterile
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NEMOTO Disposable Syringe Kit
NEMOTO Disposable Syringe Kit
NEMOTO Pressure Tube
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