PORTEX BLUE LINE ULTRA Tracheostomy Kit - Indonesia BPOM Medical Device Registration
PORTEX BLUE LINE ULTRA Tracheostomy Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403614390. The device is manufactured by SMITHS MEDICAL CZECH REPUBLIC A.S. from Czech Republic, 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
SMITHS MEDICAL CZECH REPUBLIC A.S.Country of Origin
Czech Republic
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
Apr 24, 2020
Expiry Date
Mar 16, 2025
Product Type
Therapeutic Anesthesia Equipment
Tracheostomy tube and tube cuff.
Non Electromedic Sterile
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