STERIMAR ALLERGIC NOSE - Indonesia BPOM Medical Device Registration
STERIMAR ALLERGIC NOSE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20704025217. The device is manufactured by CHURCH & DWIGHT UK LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is KEBAYORAN PHARMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CHURCH & DWIGHT UK LTD.Country of Origin
United Kingdom
Authorized Representative
KEBAYORAN PHARMAAR Address
Jl. Garuda No.79 Jakarta Pusat, 10610
Registration Date
Mar 31, 2022
Expiry Date
Mar 29, 2027
Product Type
Therapeutic Ear, Nose and Throat Equipment
Nasal irrigation solution
Non Electromedic Non Sterile

