PHILIPS RESPIRONICS Diagnostic System - Indonesia BPOM Medical Device Registration
PHILIPS RESPIRONICS Diagnostic System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20402511339. The device is manufactured by RESPIRONICS INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PHILIPS INDONESIA COMMERCIAL.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
RESPIRONICS INC.Country of Origin
United States
Authorized Representative
PHILIPS INDONESIA COMMERCIALAR Address
Gedung Cibis Nine Lantai 10, Jl. TB Simatupang No. 2
Registration Date
Aug 17, 2023
Expiry Date
May 11, 2027
Product Type
Monitoring Anesthesia Equipment
Apnea monitor.
Non Radiation Electromedics
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