Mediplus Guedel Airways - Indonesia BPOM Medical Device Registration
Mediplus Guedel Airways is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403420568. The device is manufactured by SHREE UMIYA SURGICAL PVT., LTD. from India, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is Magenta Biomedika.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHREE UMIYA SURGICAL PVT., LTD.Country of Origin
India
Authorized Representative
Magenta BiomedikaAR Address
Ruko Buaran Persada No. 30, Jl. Raya Soekamto, Duren Sawit
Registration Date
Aug 19, 2024
Expiry Date
Jun 01, 2026
Product Type
Therapeutic Anesthesia Equipment
Oropharyngeal airway.
Non Electromedic Sterile

