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 20902220911. The device is manufactured by NEW NORDISK A/S from Denmark, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ANUGRAH ARGON MEDICA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
NEW NORDISK A/SCountry of Origin
Denmark
Authorized Representative
ANUGRAH 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
NOVOFINE 32G 4mm
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