AESCULAP Eddy 3D Documentation System - Indonesia BPOM Medical Device Registration
AESCULAP Eddy 3D Documentation System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801025100. The device is manufactured by ZOLLNER ELECTRONIC AG. from Germany, 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
ZOLLNER ELECTRONIC AG.Country of Origin
Germany
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
Jun 03, 2024
Expiry Date
Mar 01, 2027
Product Type
Diagnostic Gastroenterology-Urology Equipment
Endoscope and accessories
Non Radiation Electromedics
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