LMA Proseal - Indonesia BPOM Medical Device Registration
LMA Proseal is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403614465. The device is manufactured by PARKER HANNIFIN CSS MERRILLVILLE from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. IDS MEDICAL SYSTEMS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
PARKER HANNIFIN CSS MERRILLVILLECountry of Origin
United States
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
Oct 29, 2021
Expiry Date
Dec 31, 2023
Product Type
Therapeutic Anesthesia Equipment
Tracheal tube.
Non Electromedic Non Sterile
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