GREATCARE Manual Resuscitator - Indonesia BPOM Medical Device Registration
GREATCARE Manual Resuscitator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403127493. The device is manufactured by NINGBO GREATCARE TRADING CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is LUMARY BIRUMAS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
NINGBO GREATCARE TRADING CO.,LTDCountry of Origin
China
Authorized Representative
LUMARY BIRUMASAR Address
Gd. Menara Palma Lt. 12 Jl. H.R. Rasuna Said Blok X-2, Kav.6 Jakarta 12950
Registration Date
May 14, 2024
Expiry Date
Apr 19, 2029
Product Type
Therapeutic Anesthesia Equipment
Manual emergency ventilator.
Non Electromedic Non Sterile

