ORDISI Aspirator Suction Pump - Indonesia BPOM Medical Device Registration
ORDISI Aspirator Suction Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603312728. The device is manufactured by ORDISI S.A. from Spain, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MANDIRI JAYA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ORDISI S.A.Country of Origin
Spain
Authorized Representative
PT. MANDIRI JAYA MEDIKAAR Address
Graha Mas Fatmawati Blok B No. 20, Jl. RS. Fatmawati No. 71
Registration Date
Mar 06, 2020
Expiry Date
Sep 07, 2024
Product Type
Surgical Equipment
Powered suction pump.
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