FEMITIA SENSIPACK Personal Pregnancy Test Cassette - Indonesia BPOM Medical Device Registration
FEMITIA SENSIPACK Personal Pregnancy Test Cassette is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101718675. The device is manufactured by CORE TECHNOLOGY 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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FEMITIA SENSIPACK Kaset Uji Kehamilan Pribadi
Risk Classification
Product Class
Kelas : 2
Manufacturer
CORE TECHNOLOGY CO., LTD.Country of Origin
China
Authorized Representative
PT. TUNGGAL SILA FARMAAR Address
Jl. Jend. A. Yani No. 2
Registration Date
Mar 24, 2023
Expiry Date
Jul 10, 2025
Product Type
Clinical Chemistry Test System
Human chorionic gonadotropin (HCG) test system
Invitro Diagnostics
