Portex BLUperc Percutaneous Dilation Tracheostomy Kit - Indonesia BPOM Medical Device Registration
Portex BLUperc Percutaneous Dilation Tracheostomy Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403420031. 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 IDS MEDICAL SYSTEMS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SMITHS MEDICAL CZECH REPUBLIC A.SCountry of Origin
Czech Republic
Authorized Representative
IDS MEDICAL SYSTEMS INDONESIAAR Address
Gedung Wisma 76, Lantai 17 & 22, Jl. LetJend. S. Parman Kav.76, Kelurahan Slipi, Kecamatan Palmerah, 11410
Registration Date
Feb 01, 2025
Expiry Date
Nov 22, 2029
Product Type
Therapeutic Anesthesia Equipment
Tracheostomy tube and tube cuff.
Non Electromedic Sterile
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