B. BRAUN Stimuplex Ultra 360 - Indonesia BPOM Medical Device Registration
B. BRAUN Stimuplex Ultra 360 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403710630. The device is manufactured by B. BRAUN AESCULAP JAPAN CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is B. BRAUN MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
B. BRAUN AESCULAP JAPAN CO., LTD.Country of Origin
Japan
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
Aug 21, 2024
Expiry Date
Mar 31, 2029
Product Type
Therapeutic Anesthesia Equipment
Anesthesia conduction needle.
Non Electromedic Non Sterile
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