DLP Aortic Root Cannula with Vent Line - Indonesia BPOM Medical Device Registration
DLP Aortic Root Cannula with Vent Line is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504515940. 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 MEDTRONIC INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
VIANT MEDICAL INC.Country of Origin
United States
Authorized Representative
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 16, 2023
Expiry Date
Feb 07, 2028
Product Type
Surgical Cardiology Equipment
Cardiopulmonary bypass vascular catheter, cannula, or tubing.
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