RTM3 - Indonesia BPOM Medical Device Registration
RTM3 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10402220055. The device is manufactured by MEDICAL TECHNOLOGY from France, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. IDS MEDICAL SYSTEMS INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
MEDICAL TECHNOLOGYCountry of Origin
France
Authorized Representative
PT. IDS MEDICAL SYSTEMS INDONESIAAR Address
Gedung Wisma 76, Lantai 17 & 22, Jl. LetJend. S. Parman Kav.76, Kelurahan Slipi, Kecamatan Palmerah, 11410
Registration Date
Dec 06, 2022
Expiry Date
Dec 31, 2025
Product Type
Monitoring Anesthesia Equipment
Compensated thorpe tube flowmeter.
Non Electromedic Non Sterile
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