AESCULAP Acculan 4 Traumatology - Indonesia BPOM Medical Device Registration
AESCULAP Acculan 4 Traumatology is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603918047. The device is manufactured by AESCULAP AG from Germany, and is classified as Risk Class Kelas Resiko : B. 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 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
Nov 13, 2024
Expiry Date
Mar 01, 2027
Product Type
Surgical Equipment
Surgical instrument motors and accessories/attachments.
Non Radiation Electromedics
AESCULAPยฎ Acculan 4 Orthopaedic
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AESCULAP Implant Removal Kit Set 2
AESCULAP Episiotomy Instruments Set
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AESCULAP Micro-Line and Accessories
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