CORODYN Monitoring Wedge Pressure Balloon Flotation Catheter - Indonesia BPOM Medical Device Registration
CORODYN Monitoring Wedge Pressure Balloon Flotation Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501711553. The device is manufactured by AESCULAP CHIFA SP. Z.O.O. from Poland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. B. BRAUN MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
AESCULAP CHIFA SP. Z.O.O.Country of Origin
Poland
Authorized Representative
PT. B. BRAUN MEDICAL INDONESIAAR Address
Gedung Tempo Scan Tower Lantai 30, Jl. HR Rasuna Said Kav. 3-4 RT 009 RW 004 Kel. Kuningan Timur, Kec. Setiabudi, Kota Administrasi Jakarta Selatan
Registration Date
Apr 01, 2021
Expiry Date
Aug 03, 2025
Product Type
Diagnostic Cardiology Equipment
Diagnostic intravascular catheter.
Non Electromedic Sterile
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