SENTINEL Pancreatic Amylase - Indonesia BPOM Medical Device Registration
SENTINEL Pancreatic Amylase is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101220399. The device is manufactured by SENTINEL CH. SPA from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SIEMENS HEALTHINEERS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SENTINEL CH. SPACountry of Origin
Italy
Authorized Representative
PT. SIEMENS HEALTHINEERS INDONESIAAR Address
Perkantoran Hijau Arkadia Tower F, Lantai 18, Jl. Tahi Bonar Simatupang Kav. 88, Kel. Kebagusan, Kec. Pasar Minggu, Jakarta Selatan, DKI Jakarta
Registration Date
Mar 29, 2022
Expiry Date
Jan 02, 2025
Product Type
Clinical Chemistry Test System
Amylase test system (kit & cair)
Invitro Diagnostics
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