CAPSURE ™ EPI - Indonesia BPOM Medical Device Registration
CAPSURE ™ EPI is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503413590. The device is manufactured by MEDTRONIC PUERTO RICO OPERATIONS CO., VILLALBA from United States, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MEDTRONIC INDONESIA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
MEDTRONIC PUERTO RICO OPERATIONS CO., VILLALBACountry 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
Mar 29, 2024
Expiry Date
Feb 07, 2028
Product Type
Prosthetic Cardiology Equipment
Cardiovascular permanent pacemaker electrode.
Non Electromedic Sterile
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