FISHER & PAYKEL Optiflow Nasal Cannula - Indonesia BPOM Medical Device Registration
FISHER & PAYKEL Optiflow Nasal Cannula is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403811303. The device is manufactured by FISHER & PAYKEL HEALTHCARE LTD. from New Zealand, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is MURSMEDIC.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 1
Manufacturer
FISHER & PAYKEL HEALTHCARE LTD.Country of Origin
New Zealand
Authorized Representative
MURSMEDICAR Address
Jl. Bukit Gading Raya, Komplek Gading Bukit Indah Blok SA No. 6, Kelurahan Kelapa Gading Barat
Registration Date
Jul 29, 2022
Expiry Date
May 19, 2025
Product Type
Therapeutic Anesthesia Equipment
Nasal oxygen cannula.
Non Electromedic Non Sterile
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