ZENTECH Extraction Buffer - Indonesia BPOM Medical Device Registration
ZENTECH Extraction Buffer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204911708. The device is manufactured by ZENTECH S.A from Belgium, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. FAITHFUL MEDICAL GRACE.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
ZENTECH S.ACountry of Origin
Belgium
Authorized Representative
PT. FAITHFUL MEDICAL GRACEAR Address
Mitra Sunter Boulevard Blok B No.39 Jl. Yos Sudarso Kav. 89
Registration Date
Nov 26, 2021
Expiry Date
Jul 02, 2026
Product Type
Reagents and Specimen Providers
General purpose reagent.
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