DLP® Silicone RSCP Cannulae with Manual Inflate Cuff - Indonesia BPOM Medical Device Registration
DLP® Silicone RSCP Cannulae with Manual Inflate Cuff is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504710699. 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
Nov 23, 2024
Expiry Date
Feb 19, 2029
Product Type
Surgical Cardiology Equipment
Cardiopulmonary bypass vascular catheter, cannula, or tubing.
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