SQUID18 Liquid Embolic Agent - Indonesia BPOM Medical Device Registration
SQUID18 Liquid Embolic Agent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31003812479. The device is manufactured by EMBO-FLUSSIGKEITEN A.G. from Switzerland, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is MEDIKON MAIN PHARMALAB.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
EMBO-FLUSSIGKEITEN A.G.Country of Origin
Switzerland
Authorized Representative
MEDIKON MAIN PHARMALABAR Address
JLN. RAYA PASAR MINGGU NO 15, RT.001/07
Registration Date
Sep 21, 2023
Expiry Date
Dec 31, 2025
Product Type
Therapeutic Neurology Equipment
Neurovascular embolization device.
Non Electromedic Sterile
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