PHILIPS IntelliSpace Perinatal - Indonesia BPOM Medical Device Registration
PHILIPS IntelliSpace Perinatal is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21101027899. The device is manufactured by PHILIPS MEDICAL SYSTEMS from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PHILIPS INDONESIA COMMERCIAL.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
PHILIPS MEDICAL SYSTEMSCountry of Origin
United States
Authorized Representative
PT. PHILIPS INDONESIA COMMERCIALAR Address
Gedung Cibis Nine Lantai 10, Jl. T.B. Simatupang No. 2 RT 001 RW 005
Registration Date
Nov 12, 2024
Expiry Date
Mar 13, 2029
Product Type
Obstetric and Gynecological Monitoring Equipment
Perinatal monitoring system and accessories.
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