FLEXICARE Guedel - Indonesia BPOM Medical Device Registration
FLEXICARE Guedel is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403025196. The device is manufactured by FLEXICARE MEDICAL (DONGGUAN) LIMITED from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BINABAKTI NIAGAPERKASA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
FLEXICARE MEDICAL (DONGGUAN) LIMITEDCountry of Origin
China
Authorized Representative
PT. BINABAKTI NIAGAPERKASAAR Address
Jl. Kebon Jeruk I No. 32 Taman Sari Jakarta Barat
Registration Date
Jul 29, 2022
Expiry Date
Jan 21, 2025
Product Type
Therapeutic Anesthesia Equipment
Oropharyngeal airway
Non Electromedic Sterile
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FLEXICARE Urimeter
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FLEXICARE Veoflo High Flow Nasal Cannula With Adapter
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VENTISEAL Oral Nasal ET Tube
FLEXICARE MEDICAL LIMITED