F&P NIVAIRO+/VISAIRO - Indonesia BPOM Medical Device Registration
F&P NIVAIRO+/VISAIRO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403321610. The device is manufactured by FISHER & PAYKEL HEALTHCARE S.A. DE C.V. from Mexico, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FISHER AND PAYKEL HEALTHCARE INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FISHER & PAYKEL HEALTHCARE S.A. DE C.V.Country of Origin
Mexico
Authorized Representative
PT. FISHER AND PAYKEL HEALTHCARE INDONESIAAR Address
Gandaria 8 Office Tower Lantai 8 Jl. Sultan Iskandar Muda, No.10, RT.10/RW.6. Kec. Kebayoran Lama, Jakarta Selatan 12240, Indonesia.
Registration Date
Sep 26, 2023
Expiry Date
Jun 26, 2028
Product Type
Therapeutic Anesthesia Equipment
Positive airway pressure delivery system
Non Electromedic Non Sterile
