GC TOOTH MOUSSE - Indonesia BPOM Medical Device Registration
GC TOOTH MOUSSE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20604320174. The device is manufactured by GC AMERICA INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PHARMINDO LESTARI AWARD.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GC AMERICA INC.Country of Origin
United States
Authorized Representative
PHARMINDO LESTARI AWARDAR Address
Jl. Boulevard BGR No. 1, Komplek Pergudangan BGR Gudang M, Kel. Kelapa Gading Barat, Kec. Kelapa Gading, Jakarta Utara, DKI Jakarta
Registration Date
Jun 27, 2023
Expiry Date
Oct 14, 2026
Product Type
Therapeutic Dental Equipment
Oral rinse to reduce the adhesion of dental plaque.
Non Electromedic Non Sterile
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