AESCULAP Electrosurgical Endoscopy Equipment - Indonesia BPOM Medical Device Registration
AESCULAP Electrosurgical Endoscopy Equipment is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20804420142. The device is manufactured by AESCULAP AG from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. B. BRAUN MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
AESCULAP AGCountry of Origin
Germany
Authorized Representative
PT. B. BRAUN MEDICAL INDONESIAAR Address
GEDUNG TEMPO SCAN LANTAI 30, JL H.R. RASUNA SAID KAV.3-4
Registration Date
Dec 26, 2024
Expiry Date
Mar 01, 2027
Product Type
Gastroenterology-Surgical Urology Equipment
Endoscopic electrosurgical unit and accessories.
Non Electromedic Non Sterile
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