FEMITIA SensiPlan - Indonesia BPOM Medical Device Registration
FEMITIA SensiPlan is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101221111. 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.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
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
Jul 28, 2022
Expiry Date
Jul 26, 2025
Product Type
Clinical Chemistry Test System
Luteinizing hormone test system (strip & midstream)
Invitro Diagnostics
