GOLDENWELL Flashback Blood Collection Needle - Indonesia BPOM Medical Device Registration
GOLDENWELL Flashback Blood Collection Needle is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902420528. The device is manufactured by YANGZHOU GOLDENWELL MEDICAL DEVICES FACTORY from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. VIPRO MEDITECH PRATAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
YANGZHOU GOLDENWELL MEDICAL DEVICES FACTORYCountry of Origin
China
Authorized Representative
PT. VIPRO MEDITECH PRATAMAAR Address
Puri Metropolitan Blok G1 No. 21 RT 005 RW 007.
Registration Date
May 31, 2024
Expiry Date
Jan 12, 2029
Product Type
Therapeutic General and Individual Hospital Equipment
Hypodermic single lumen needle.
Non Electromedic Sterile
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