FCI BIKA Bicanalicular Intubation Set for DCR - Indonesia BPOM Medical Device Registration
FCI BIKA Bicanalicular Intubation Set for DCR is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203816283. The device is manufactured by FRANCE CHIRURGIE INSTRUMENTATION SAS ( FCI S.A.S. ) from France, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEGA MEDICAL ABADI.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
France
Authorized Representative
PT. MEGA MEDICAL ABADIAR Address
Komplek Fatmawati Mas Blok B5 Kav. 207-208, Jl. RS. Fatmawati No. 20, RT. 005 RW. 010
Registration Date
Oct 31, 2023
Expiry Date
Oct 01, 2026
Product Type
Surgical Eye Equipment
Nasal Binacalicular Intubation
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