IISM Vein Probe - Indonesia BPOM Medical Device Registration
IISM Vein Probe is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10903814005. The device is manufactured by IISM INC. from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is SERENITY INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
IISM INC.Country of Origin
Korea
Authorized Representative
SERENITY INDONESIAAR Address
Komp. Ruko Griya Inti Sentosa Jl. Griya Agung Blok O No. 96 Sunter
Registration Date
Sep 01, 2022
Expiry Date
Jan 01, 2025
Product Type
General Hospital Equipment and Other Individuals
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