AXIMED® Lancing Device - Indonesia BPOM Medical Device Registration
AXIMED® Lancing Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603110934. The device is manufactured by HUAIAN TIANDA MEDICAL INSTRUMENTS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BIO AXION HEALTHINDO.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
HUAIAN TIANDA MEDICAL INSTRUMENTS CO., LTD.Country of Origin
China
Authorized Representative
PT. BIO AXION HEALTHINDOAR Address
Komplek golden plaza Blok E-43, Jl. RS.Fatmawati no.15. Jakarta Selatan
Registration Date
Mar 20, 2019
Expiry Date
Mar 04, 2024
Product Type
Surgical Equipment
Manual surgical instrument for general use.
Non Electromedic Sterile
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GEA Sterile Surgical Blades
GEA Blood Lancet
GENERAL CARE Surgical Blade
GENERAL CARE Lancing Device with Blood Lancet
GEA Sterile Blood Lancet
GEA Blood Lancing Device
GEA Sterile Blood Lancet
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AXIMED Paper Tape
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AXIMED® Lancet
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AXIMED Rectal Tube
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