FEMITIA FEMIJECT DUO - Indonesia BPOM Medical Device Registration
FEMITIA FEMIJECT DUO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902221416. The device is manufactured by WUXI YUSHOU MEDICAL APPLIANCES CO LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TUNGGAL SILA FARMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
WUXI YUSHOU MEDICAL APPLIANCES CO LTDCountry of Origin
China
Authorized Representative
PT. TUNGGAL SILA FARMAAR Address
Jl. Jend. A. Yani No. 2
Registration Date
Dec 16, 2022
Expiry Date
Dec 14, 2025
Product Type
Therapeutic General and Individual Hospital Equipment
Piston syringe.
Non Electromedic Sterile

