FEMITIA SENSIJECT DUO - Indonesia BPOM Medical Device Registration
FEMITIA SENSIJECT DUO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902911499. The device is manufactured by JIANGXI HONGDA MEDICAL EQUIPMENT GROUP 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
JIANGXI HONGDA MEDICAL EQUIPMENT GROUP LTD.Country of Origin
China
Authorized Representative
PT. TUNGGAL SILA FARMAAR Address
Jl. Jend. A. Yani No. 2
Registration Date
Feb 18, 2022
Expiry Date
Feb 18, 2025
Product Type
Therapeutic General and Individual Hospital Equipment
Piston syringe.
Non Electromedic Sterile
