PHOENIX Nasal CPAP 300 - Indonesia BPOM Medical Device Registration
PHOENIX Nasal CPAP 300 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403126986. The device is manufactured by PHOENIX MEDICAL SYSTEMS PRIVATE LIMITED from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEDMAX GLOBAL INDOTAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
PHOENIX MEDICAL SYSTEMS PRIVATE LIMITEDCountry of Origin
India
Authorized Representative
PT. MEDMAX GLOBAL INDOTAMAAR Address
Perum Taman Candiloka C3-7 Ngampelsari Candi Sidoarjo
Registration Date
Nov 16, 2021
Expiry Date
Jul 30, 2024
Product Type
Therapeutic Anesthesia Equipment
Positive airway pressure delivery system
Non Radiation Electromedics
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