GUM Pro's Interdental Brush L-Type - Indonesia BPOM Medical Device Registration
GUM Pro's Interdental Brush L-Type is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10605520021. The device is manufactured by YAMATO-ESULON (THAILAND) CO., LTD. from Thailand, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is MEGA MEDICAL ABADI.
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GUM Proโs Interdental Brush L-Type
Risk Classification
Product Class
Kelas : 1
Manufacturer
YAMATO-ESULON (THAILAND) CO., LTD.Country of Origin
Thailand
Authorized Representative
MEGA MEDICAL ABADIAR Address
Komplek Fatmawati Mas Blok B5 Kav. 207-208, Jl. RS. Fatmawati No. 20, RT. 005 RW. 010
Registration Date
Jan 14, 2025
Expiry Date
Aug 31, 2029
Product Type
Other Dental Equipment
Manual toothbrush.
Non Electromedic Non Sterile
GUM Pro's Interdental Brush L-Type SSS
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