SENTINEL Ammonia Ultra - Indonesia BPOM Medical Device Registration
SENTINEL Ammonia Ultra is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101025234. 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. ABBOTT PRODUCTS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SENTINEL CH. SPA.Country of Origin
Italy
Authorized Representative
PT. ABBOTT PRODUCTS INDONESIAAR Address
Wisma Pondok Indah 2, Suite 1000, Jl. Sultan Iskandar Muda Kav V - TA
Registration Date
Dec 02, 2024
Expiry Date
Oct 28, 2029
Product Type
Clinical Chemistry Test System
Ammonia test system (kit & cair)
Invitro Diagnostics
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