NOVOFINE Plus, 32G 4mm - Indonesia BPOM Medical Device Registration
NOVOFINE Plus, 32G 4mm is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902220928. The device is manufactured by NIPRO MEDICAL INDUSTRIES LTD. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GRACE ARGON MEDICA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
NIPRO MEDICAL INDUSTRIES LTD.Country of Origin
Japan
Authorized Representative
PT. GRACE ARGON MEDICAAR Address
Titan Center Lantai 4, Jl. Boulevard Bintaro Blok B7/B1 No. 5 Bintaro Jaya Sektor 7
Registration Date
Dec 30, 2024
Expiry Date
Mar 31, 2029
Product Type
Therapeutic General and Individual Hospital Equipment
Hypodermic single lumen needle.
Non Electromedic Sterile
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