ULTRAVERSE 035 PTA Dilation Catheter - Indonesia BPOM Medical Device Registration
ULTRAVERSE 035 PTA Dilation Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501124607. The device is manufactured by CLEARSTREAM TECHNOLOGIES LTD. from Ireland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ITAMA RANORAYA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CLEARSTREAM TECHNOLOGIES LTD.Country of Origin
Ireland
Authorized Representative
PT. ITAMA RANORAYAAR Address
MT Haryono Square Lantai 1 Unit 1, Jl. Otto Iskandardinata Raya No. 390 RT 006 RW 012 Kel. Bidara Cina, Kec. Jatinegara, Jakarta Timur, DKI Jakarta
Registration Date
Jul 30, 2021
Expiry Date
Dec 31, 2025
Product Type
Diagnostic Cardiology Equipment
Percutaneous catheter.
Non Electromedic Sterile
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