FARGO Guiding Catheters - Indonesia BPOM Medical Device Registration
FARGO Guiding Catheters is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501611508. The device is manufactured by BALT EXTRUSION SAS. from France, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is MEDIKON MAIN PHARMALAB.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BALT EXTRUSION SAS.Country of Origin
France
Authorized Representative
MEDIKON MAIN PHARMALABAR Address
JLN. RAYA PASAR MINGGU NO 15, RT.001/07
Registration Date
Oct 10, 2024
Expiry Date
Dec 31, 2027
Product Type
Diagnostic Cardiology Equipment
Catheter guide wire.
Non Electromedic Sterile
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