TRANSFORM Occlusion Ballon Catheter - Indonesia BPOM Medical Device Registration
TRANSFORM Occlusion Ballon Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31003127790. The device is manufactured by STRYKER NEUROVASCULAR from Ireland, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is WICAKSANA OVERSEAS INTERNATIONAL.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
STRYKER NEUROVASCULARCountry of Origin
Ireland
Authorized Representative
WICAKSANA OVERSEAS INTERNATIONALAR Address
Jl. Ancol Barat VII Blok A5/D No. 2 RT 006 RW 001
Registration Date
Mar 01, 2022
Expiry Date
Jan 31, 2024
Product Type
Therapeutic Neurology Equipment
Intravascular occluding catheter.
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