AGAPPE Mispa I2 RF - Indonesia BPOM Medical Device Registration
AGAPPE Mispa I2 RF is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305220105. The device is manufactured by AGAPPE DIAGNOSTICS SWITZERLAND GMBH. from Switzerland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MULTIMEDILAB KARYAMANDIRI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
AGAPPE DIAGNOSTICS SWITZERLAND GMBH.Country of Origin
Switzerland
Authorized Representative
PT. MULTIMEDILAB KARYAMANDIRIAR Address
GP plaza lantai 3 unit 6, jalan Gelora II No. 01
Registration Date
Apr 04, 2022
Expiry Date
Dec 16, 2025
Product Type
Immunological Test System
Rheumatoid factor immunological test system.
Invitro Diagnostics
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