B. BRAUN Inflation Device - Indonesia BPOM Medical Device Registration
B. BRAUN Inflation Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501713784. 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 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
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
Oct 04, 2023
Expiry Date
Aug 18, 2027
Product Type
Diagnostic Cardiology Equipment
Angiographic injector and syringe.
Non Electromedic Sterile
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