GUM Post Operation Tootbrush - Indonesia BPOM Medical Device Registration
GUM Post Operation Tootbrush is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10605917913. The device is manufactured by SUNSTAR AMERICAS, INC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is MULTI MEDIKA RAYA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
SUNSTAR AMERICAS, INC.Country of Origin
United States
Authorized Representative
MULTI MEDIKA RAYAAR Address
CITYPARK BUSINESS DISTRICT (CBD) BLOK E1/8 CENGKARENG TIMUR JAKARTA 11730
Registration Date
Dec 06, 2019
Expiry Date
Aug 19, 2024
Product Type
Other Dental Equipment
Manual toothbrush.
Non Electromedic Non Sterile
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