MARIMER - Hypertonic Sea Water Solution, Nasal Spr - Indonesia BPOM Medical Device Registration
MARIMER - Hypertonic Sea Water Solution, Nasal Spr is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20704613433. The device is manufactured by LABORATORY OF THE SEA from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PHAPROS, TBK..
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LABORATORY OF THE SEACountry of Origin
France
Authorized Representative
PT. PHAPROS, TBK.AR Address
GD. RNI, JL. DENPASAR RAYA KAV. D-III KUNINGAN TIMUR, SETIABUDI, JAKARTA SELATAN
Registration Date
Sep 15, 2020
Expiry Date
Jul 22, 2025
Product Type
Therapeutic Ear, Nose and Throat Equipment
Nasal irrigation solution
Non Electromedic Non Sterile

