VICOM Sterile Syringe For Single Use - Indonesia BPOM Medical Device Registration
VICOM Sterile Syringe For Single Use is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902123870. The device is manufactured by SHANGHAI KINDLY ENTERPRISE DEVELOPMENT GROUP CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PRIMARY WORKS.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
China
Authorized Representative
PT. PRIMARY WORKSAR Address
Daan Mogot Arcadia Blok F.1/8A-8B Jl. Daan Mogot Km 21, Kelurahan Batu Ceper
Registration Date
Jul 01, 2021
Expiry Date
Jul 01, 2024
Product Type
Therapeutic General and Individual Hospital Equipment
Piston syringe.
Non Electromedic Sterile
VICOM Sterile Syringe For Single Use
SHANGHAI KINDLY ENTERPRISE DEVELOPMENT GROUP CO., LTD.
VICOM Sterile Syringe For Single Use
SHANGHAI KINDLY ENTERPRISE DEVELOPMENT GROUP CO., LTD.
VICOM Sterile Syringe For Single Use
SHANGHAI KINDLY ENTERPRISE DEVELOPMENT GROUP CO., LTD.
VICOM Sterile Syringe For Single Use
SHANGHAI KINDLY ENTERPRISE DEVELOPMENT GROUP CO., LTD.
VICOM Sterile Syringe For Single Use
SHANGHAI KINDLY ENTERPRISE DEVELOPMENT GROUP CO., LTD.
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