B. BRAUN Angiodyn HK Kit - Indonesia BPOM Medical Device Registration
B. BRAUN Angiodyn HK Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603814485. The device is manufactured by AESCULAP CHIFA SP. Z.O.O. from Poland, and is classified as Risk Class Kelas Resiko : B. 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 06, 2022
Expiry Date
Jan 07, 2024
Product Type
Surgical Equipment
Surgical drape and drape accessories.
Non Electromedic Sterile
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