FISHER & PAYKEL Optiflow Tracheostomy Direct Connection - Indonesia BPOM Medical Device Registration
FISHER & PAYKEL Optiflow Tracheostomy Direct Connection is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403812304. The device is manufactured by FISHER & PAYKEL HEALTHCARE LTD. from New Zealand, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MURSMEDIC.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FISHER & PAYKEL HEALTHCARE LTD.Country of Origin
New Zealand
Authorized Representative
PT. MURSMEDICAR Address
The Kensington Office Tower Lantai 11, Jalan Boulevard Raya Nomor 1, Desa/Kelurahan Kelapa Gading Timur, Kec. Kelapa Gading, Kota Adm. Jakarta Utara, Provinsi DKI Jakarta, 14240
Registration Date
Feb 07, 2025
Expiry Date
Oct 14, 2029
Product Type
Therapeutic Anesthesia Equipment
Respiratory gas humidifier.
Non Electromedic Non Sterile
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