VIDA Disposable Syringe 50ml - Indonesia BPOM Medical Device Registration
VIDA Disposable Syringe 50ml is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902420982. The device is manufactured by SHANGHAI MEDIC INDUSTRY CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DANVI MEDILAB PERKASA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHANGHAI MEDIC INDUSTRY CO., LTDCountry of Origin
China
Authorized Representative
PT. DANVI MEDILAB PERKASAAR Address
Jl. Kapten Muslim Komp. Mega Com Center Blok G No. 1-2 Kel. Dwikora Kec. Medan Helvetia
Registration Date
Dec 13, 2024
Expiry Date
Sep 06, 2027
Product Type
Therapeutic General and Individual Hospital Equipment
Piston syringe.
Non Electromedic Sterile
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