ONIONEX Infusion Set for Adult - Indonesia BPOM Medical Device Registration
ONIONEX Infusion Set for Adult is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902122113. The device is manufactured by SHANDONG YIGUANG MEDICAL INSTRUMENTS CO., LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PRIMA ALKESINDO NUSANTARA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHANDONG YIGUANG MEDICAL INSTRUMENTS CO., LTDCountry of Origin
China
Authorized Representative
PT. PRIMA ALKESINDO NUSANTARAAR Address
Jl. Bukit Gading Raya Blok C 12 - C 15 Kel. Kelapa Gading Barat, Kec. Kelapa Gading, Jakarta Utara
Registration Date
Apr 13, 2021
Expiry Date
Apr 13, 2024
Product Type
Therapeutic General and Individual Hospital Equipment
Intravascular administration set.
Non Electromedic Sterile
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