RADISTOP ™ Compression Assist Device - Indonesia BPOM Medical Device Registration
RADISTOP ™ Compression Assist Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11604916986. The device is manufactured by ST. JUDE MEDICAL PUERTO RICO, LLC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. TAWADA HEALTHCARE.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
ST. JUDE MEDICAL PUERTO RICO, LLC.Country of Origin
United States
Authorized Representative
PT. TAWADA HEALTHCAREAR Address
RUKAN PERMATA SENAYAN BLOK A18-19 JL. TENTARA PELAJAR NO. 5
Registration Date
Oct 28, 2019
Expiry Date
Aug 01, 2024
Product Type
Therapeutic Surgical Equipment
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