INTER Patient Monitor - Indonesia BPOM Medical Device Registration
INTER Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502220164. The device is manufactured by UTECH CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. AMBRA ANUBAWA BERSAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
UTECH CO.,LTDCountry of Origin
China
Authorized Representative
PT. AMBRA ANUBAWA BERSAMAAR Address
JI. KIhajar Dewantara Ruko Golden 8 Blok A. No. 7 Gading Serpong Summarecon Tangerang Banten 15810 Tlp. 021. 29238848
Registration Date
May 19, 2022
Expiry Date
May 18, 2025
Product Type
Monitoring Cardiology Equipment
Cardiac monitor (including cardiotachometer and rate alarm).
Non Radiation Electromedics

