DEWIMED Suction Tube Instruments - Indonesia BPOM Medical Device Registration
DEWIMED Suction Tube Instruments is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903613709. The device is manufactured by DEWIMED MEDIZINTECHNIK GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is JEMA INDO MANDIRI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DEWIMED MEDIZINTECHNIK GMBHCountry of Origin
Germany
Authorized Representative
JEMA INDO MANDIRIAR Address
Jl. RS. Fatmawati No. 100 E Cilandak Jakarta Selatan
Registration Date
Feb 24, 2023
Expiry Date
Dec 31, 2025
Product Type
General Hospital Equipment and Other Individuals
Vacuum-powered body fluid suction apparatus.
Non Electromedic Non Sterile
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