PRYMAX Perfusion - Venous Cannula - Indonesia BPOM Medical Device Registration
PRYMAX Perfusion - Venous Cannula is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504120831. The device is manufactured by PRYMAX HEALTHCARE LLP from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is BISAWI GROWS IN HARMONY.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
PRYMAX HEALTHCARE LLPCountry of Origin
India
Authorized Representative
BISAWI GROWS IN HARMONYAR Address
Graha Kencana Blok EU Jl. Raya Perjuangan No.88 Kebun Jeruk Jakarta Barat
Registration Date
Sep 17, 2024
Expiry Date
Sep 08, 2028
Product Type
Surgical Cardiology Equipment
Cardiopulmonary bypass vascular catheter, cannula, or tubing.
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