NEW Bililed Maxi - Indonesia BPOM Medical Device Registration
NEW Bililed Maxi is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902220527. The device is manufactured by NOVOS TIBBI CIHAZLAR SAN. VE TIC. ITH. AND IHR. LTD. ลTI from Turkey, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SEKARGUNA MEDIKA.
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NOVOS Bililed Maxi
Risk Classification
Product Class
Kelas : 2
Country of Origin
Turkey
Authorized Representative
PT. SEKARGUNA MEDIKAAR Address
jl.Ciputat Raya no 14 B.Pondok Pinang
Registration Date
Jun 06, 2022
Expiry Date
Jan 03, 2027
Product Type
Therapeutic General and Individual Hospital Equipment
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