AESCULAP Cranioplasty Set - Indonesia BPOM Medical Device Registration
AESCULAP Cranioplasty Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11002817324. 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 14, 2025
Expiry Date
Mar 01, 2027
Product Type
Surgical Neurology Equipment
Nonpowered neurosurgical instrument.
Non Electromedic Non Sterile
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AESCULAP Multi Interchangeable Trocar System
AESCULAP Gynaecology Scissors
AESCULAP Kerrison & Rodents set
AESCULAP Transphenoidal Instrument Set
AESCULAP DS Ligation Clips
AESCULAP Saw Blades
AESCULAP Aneurysm Clip Set
AESCULAP Tracheotomy Instrument
AESCULAP Fine Wound Retractor
AESCULAP Kerrison & Rodents set
AESCULAP AG.
AESCULAP Transphenoidal Instrument Set
AESCULAP AG.
AESCULAP DS Ligation Clips
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AESCULAP Aneurysm Clip Set
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AESCULAP Tracheotomy Instrument
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AESCULAP® Acculan 4 Orthopaedic
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AESCULAP Craniotomy Set
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AESCULAP Caspar Cervical Retractor System
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AESCULAP Laminectomy set
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AESCULAP Laparascopy Surgery
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