PRUITT Aortic Occlusion Catheter - Indonesia BPOM Medical Device Registration
PRUITT Aortic Occlusion Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501220294. The device is manufactured by LEMAITRE VASCULAR, INC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GEM OF GRACE VIBRASA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LEMAITRE VASCULAR, INCCountry of Origin
United States
Authorized Representative
PT. GEM OF GRACE VIBRASAAR Address
Perkantoran CBD Ciledug Jl. Hos Cokroaminoto No. 93 Ruko perkantoran CBD Ciledug Blok A3 No. 28
Registration Date
Jul 07, 2022
Expiry Date
Apr 21, 2026
Product Type
Diagnostic Cardiology Equipment
Catheter tip occluder.
Non Electromedic Sterile
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