BEX Guedel Airway - Indonesia BPOM Medical Device Registration
BEX Guedel Airway is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403220662. The device is manufactured by BIÇAKCILAR TIBBI CIHAZLAR SANAYI VE TICARET A.S. from Turkey, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. PERUSAHAAN PERSEROAN (PERSERO) INDONESIA FARMA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
BIÇAKCILAR TIBBI CIHAZLAR SANAYI VE TICARET A.S.Country of Origin
Turkey
Authorized Representative
PT. PERUSAHAAN PERSEROAN (PERSERO) INDONESIA FARMAAR Address
Jl. Tambak No. 2 RT 013 RW 008
Registration Date
Sep 09, 2022
Expiry Date
Dec 31, 2023
Product Type
Therapeutic Anesthesia Equipment
Oropharyngeal airway
Non Electromedic Sterile
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