VTEK Automatic Reusable Biopsy Device - Indonesia BPOM Medical Device Registration
VTEK Automatic Reusable Biopsy Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801915471. The device is manufactured by VIGEO S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BRIDGE TWO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
VIGEO S.R.L.Country of Origin
Italy
Authorized Representative
PT. BRIDGE TWOAR Address
Jl. Petojo Melintang No. 17
Registration Date
Aug 23, 2023
Expiry Date
Jan 09, 2028
Product Type
Diagnostic Gastroenterology-Urology Equipment
Gastroenterology-urology biopsy instrument
Non Electromedic Non Sterile
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