ISOMED Huber Needle with extension - Indonesia BPOM Medical Device Registration
ISOMED Huber Needle with extension is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902021375. The device is manufactured by ISO MED S.A.R.L. from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PELITA BIOMEDICAL.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ISO MED 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 01, 2022
Expiry Date
May 06, 2027
Product Type
Therapeutic General and Individual Hospital Equipment
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