FAMILY DR. Nasal Dilator - Indonesia BPOM Medical Device Registration
FAMILY DR. Nasal Dilator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10702420053. The device is manufactured by DREAM AIR CO. LTD. from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. INDOCORE PERKASA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
DREAM AIR CO. LTD.Country of Origin
Korea
Authorized Representative
PT. INDOCORE PERKASAAR Address
Komplek Graha Mas Pemuda Blok AB No. 19, Jl. Pemuda RT 020 / RW 006
Registration Date
Jul 05, 2024
Expiry Date
Feb 06, 2029
Product Type
Prosthetic Ear, Nose and Throat Equipment
Nasal dilator.
Non Electromedic Non Sterile
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