PRESSUREWIRE™ X Guidewire - Indonesia BPOM Medical Device Registration
PRESSUREWIRE™ X Guidewire is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502023589. The device is manufactured by ABBOTT VASCULAR from Costa Rica, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is TAWADA HEALTHCARE.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ABBOTT VASCULARCountry of Origin
Costa Rica
Authorized Representative
TAWADA HEALTHCAREAR Address
Rukan Permata Senayan Blok A18-19 Lantai 1-2 Jl. Tentara Pelajar No. 5
Registration Date
May 12, 2023
Expiry Date
Feb 09, 2028
Product Type
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