INFU KT - Titanium Access Port Pression Injection - Indonesia BPOM Medical Device Registration
INFU KT - Titanium Access Port Pression Injection is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902817242. The device is manufactured by ISOMED S.A.R.L. from France, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PELITA BIOMEDICAL.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ISOMED S.A.R.L.Country of Origin
France
Authorized Representative
PT. PELITA BIOMEDICALAR Address
Gedung Autobridal Lantai4 Jl. KH Abdullah Syafei No.30 Kel. Asem Baris Kec. Tebet Jakarta Selatan
Registration Date
Nov 21, 2022
Expiry Date
May 06, 2027
Product Type
Therapeutic General and Individual Hospital Equipment
Subcutaneous, implanted, intravascular infusion port and catheter.
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