GELWEAVE Woven Vascular Prothesis - Indonesia BPOM Medical Device Registration
GELWEAVE Woven Vascular Prothesis is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20503505072. The device is manufactured by VASCUTEK LIMITED from United Kingdom, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TERUMO INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
VASCUTEK LIMITEDCountry of Origin
United Kingdom
Authorized Representative
PT. TERUMO INDONESIAAR Address
Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta
Registration Date
Aug 30, 2022
Expiry Date
May 23, 2027
Product Type
Prosthetic Cardiology Equipment
Vascular graft prosthesis.
Non Electromedic Sterile
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