GSP Neonatal 17α-OH Progesterone Kit - Indonesia BPOM Medical Device Registration
GSP Neonatal 17α-OH Progesterone Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101123148. The device is manufactured by WALLAC OY from Finland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. UBC MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
WALLAC OYCountry of Origin
Finland
Authorized Representative
PT. UBC MEDICAL INDONESIAAR Address
Jalan Rawa Gelam V, Blok L Kav. 11-13, Kawasan Industri Pulogadung Jakarta Timur13930
Registration Date
Feb 08, 2025
Expiry Date
Oct 22, 2028
Product Type
Clinical Chemistry Test System
17-Hydroxyprogesterone test system (kit & cair)
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