AESCULAP Full HD Monitor - Indonesia BPOM Medical Device Registration
AESCULAP Full HD Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801023713. The device is manufactured by DIVA LABORATORIES, LTD. from Taiwan (China), 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
DIVA LABORATORIES, LTD.Country of Origin
Taiwan (China)
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
Oct 12, 2022
Expiry Date
Nov 18, 2026
Product Type
Diagnostic Gastroenterology-Urology Equipment
Endoscope and accessories
Non Radiation Electromedics
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