AESCULAP Laminectomy set - Indonesia BPOM Medical Device Registration
AESCULAP Laminectomy set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11002816953. 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
Dec 19, 2024
Expiry Date
Mar 01, 2027
Product Type
Surgical Neurology Equipment
Nonpowered neurosurgical instrument.
Non Electromedic Non Sterile
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