IntelliSpace Perinatal Rev. K.00 - Indonesia BPOM Medical Device Registration
IntelliSpace Perinatal Rev. K.00 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21101914517. The device is manufactured by PHILIPS MEDIZIN SYSTEME BOEBLINGEN GMBH. from Germany, 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 MEDIZIN SYSTEME BOEBLINGEN GMBH.Country of Origin
Germany
Authorized Representative
PT. PHILIPS INDONESIA COMMERCIALAR Address
Gedung Cibis Nine Lantai 10 Jl. TB Simatupang No. 2 RT.001 RW. 005 Kel. Cilandak Timur Kec. Pasar Minggu Jakarta Selatan
Registration Date
Jul 29, 2019
Expiry Date
Feb 14, 2024
Product Type
Obstetric and Gynecological Monitoring Equipment
Perinatal monitoring system and accessories.
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