AESCULAP WL/FI Light Source - Indonesia BPOM Medical Device Registration
AESCULAP WL/FI Light Source is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801220490. The device is manufactured by AESCULAP AG. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is B. BRAUN MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
AESCULAP AG.Country of Origin
Germany
Authorized Representative
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
Dec 26, 2022
Expiry Date
Nov 18, 2026
Product Type
Diagnostic Gastroenterology-Urology Equipment
Endoscope and accessories
Non Radiation Electromedics
AESCULAP Scalpel & Knives
AESCULAP Multi Interchangeable Trocar System
AESCULAP Kerrison & Rodents set
AESCULAP Cranioplasty Set
AESCULAP Gynaecology Scissors
AESCULAP Transphenoidal Instrument Set
AESCULAP DS Ligation Clips
AESCULAP Saw Blades
AESCULAP Aneurysm Clip Set
AESCULAP Tracheotomy Instrument
AESCULAP Cranioplasty Set
AESCULAP AG.
AESCULAP Kerrison & Rodents set
AESCULAP AG.
AESCULAP Transphenoidal Instrument Set
AESCULAP AG.
AESCULAP DS Ligation Clips
AESCULAP AG.
AESCULAP Aneurysm Clip Set
AESCULAP AG.
AESCULAP® Acculan 4 Orthopaedic
AESCULAP AG
AESCULAP Tracheotomy Instrument
AESCULAP AG.
AESCULAP Craniotomy Set
AESCULAP AG.
AESCULAP Caspar Cervical Retractor System
AESCULAP AG.
AESCULAP Laminectomy set
AESCULAP AG.