GEA AIR / OXYGEN BLENDER - Indonesia BPOM Medical Device Registration
GEA AIR / OXYGEN BLENDER is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403022726. The device is manufactured by NINGBO DAVID MEDICAL DEVICE CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MEGA PRATAMA MEDICALINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
NINGBO DAVID MEDICAL DEVICE CO.,LTDCountry of Origin
China
Authorized Representative
MEGA PRATAMA MEDICALINDOAR Address
Jl. Pluit Raya 133 Blok A.3
Registration Date
Mar 16, 2023
Expiry Date
Jun 02, 2026
Product Type
Therapeutic Anesthesia Equipment
Breathing gas mixer.
Non Electromedic Non Sterile
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