GES BLOOD LANCET - Indonesia BPOM Medical Device Registration
GES BLOOD LANCET is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603122452. The device is manufactured by HUAIAN HELEN MEDICAL INSTRUMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. GANDASARI EKASATYA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
HUAIAN HELEN MEDICAL INSTRUMENT CO., LTD.Country of Origin
China
Authorized Representative
PT. GANDASARI EKASATYAAR Address
Jl. Raya HANKAM No.9A RT.007/002 Kel. Bambu Apus, Kec. Cipayung 13890
Registration Date
Feb 19, 2024
Expiry Date
Feb 18, 2027
Product Type
Surgical Equipment
Manual surgical instrument for general use.
Non Electromedic Sterile
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