DLP Multiple Perfusion Set - Indonesia BPOM Medical Device Registration
DLP Multiple Perfusion Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504515686. The device is manufactured by VIANT MEDICAL INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEDTRONIC INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
VIANT MEDICAL INC.Country of Origin
United States
Authorized Representative
PT. MEDTRONIC INDONESIAAR Address
Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda, Desa/Kelurahan Kebayoran Lama Utara, Kec. Kebayoran Lama
Registration Date
Oct 19, 2023
Expiry Date
Feb 06, 2028
Product Type
Surgical Cardiology Equipment
Cardiopulmonary bypass vascular catheter, cannula, or tubing.
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