GEA Spring Eye Needle - Indonesia BPOM Medical Device Registration
GEA Spring Eye Needle is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902903829. The device is manufactured by HONGZE CHENGUANG MEDICAL INSTRUMENT. CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEGA PRATAMA MEDICALINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HONGZE CHENGUANG MEDICAL INSTRUMENT. CO., LTD.Country of Origin
China
Authorized Representative
PT. MEGA PRATAMA MEDICALINDOAR Address
Jl. Pluit Raya 133 Blok A.3
Registration Date
Nov 23, 2020
Expiry Date
Nov 23, 2023
Product Type
Therapeutic General and Individual Hospital Equipment
Hypodermic single lumen needle.
Non Electromedic Sterile
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