KDL Sterile Needle For Single Use - Indonesia BPOM Medical Device Registration
KDL Sterile Needle For Single Use is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902318141. 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. CITRA PERSADA MEDICINDO.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
China
Authorized Representative
PT. CITRA PERSADA MEDICINDOAR Address
Jl. DR. Ratulangi No. 7 B-1 Makassar Sulawesi Selatan
Registration Date
Jun 14, 2020
Expiry Date
Mar 01, 2025
Product Type
Therapeutic General and Individual Hospital Equipment
Hypodermic single lumen needle.
Non Electromedic Non Sterile
KDL For Single Use Sterile Syringe 10 mL
KDL For Single Use Sterile Syringe 1 ml, 3 ml dan 5 ml
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