GlucoDr. Pen Needle - Indonesia BPOM Medical Device Registration
GlucoDr. Pen Needle is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902220917. The device is manufactured by MEDEXEL CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDISINDO BAHANA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MEDEXEL CO., LTD.Country of Origin
Korea
Authorized Representative
PT. MEDISINDO BAHANAAR Address
Rukan Graha Cempaka Mas Blok E No.15 Lt.3, Jl. Letjen Suprapto No.1, Jakarta Pusat
Registration Date
Aug 25, 2022
Expiry Date
Apr 17, 2027
Product Type
Therapeutic General and Individual Hospital Equipment
Hypodermic single lumen needle.
Non Electromedic Sterile
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