ANDINI Patient Monitor - Indonesia BPOM Medical Device Registration
ANDINI Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502510570. The device is manufactured by EDAN INSTRUMENTS, INC. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ANDINI SARANA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
EDAN INSTRUMENTS, INC.Country of Origin
China
Authorized Representative
PT. ANDINI SARANAAR Address
Jln. Rawa Sumur III, Kav. III, Blok DD No. 11. Kawasan Industri Pulogadung Jakarta Timur
Registration Date
Nov 28, 2022
Expiry Date
Dec 31, 2024
Product Type
Monitoring Cardiology Equipment
Cardiac monitor (including cardiotachometer and rate alarm).
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