AESCULAP Transphenoidal Instrument Set - Indonesia BPOM Medical Device Registration
AESCULAP Transphenoidal Instrument Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10703818268. The device is manufactured by AESCULAP AG. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is B. BRAUN MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
AESCULAP AG.Country of Origin
Germany
Authorized Representative
B. BRAUN MEDICAL INDONESIAAR Address
GEDUNG TEMPO SCAN LANTAI 30, JL H.R. RASUNA SAID KAV.3-4
Registration Date
Jan 08, 2025
Expiry Date
Mar 01, 2027
Product Type
Ear, Nose and Throat Surgical Equipment
Ear, nose, and throat manual surgical instrument.
Non Electromedic Non Sterile
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