ASCENDA INTRATHECAL CATHETER 8780 SPINAL SEGMENT - Indonesia BPOM Medical Device Registration
ASCENDA INTRATHECAL CATHETER 8780 SPINAL SEGMENT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31002817002. The device is manufactured by MEDTRONIC PUERTO RICO OPERATIONS CO. JUNCOS 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. JUNCOSCountry of Origin
United States
Authorized Representative
PT. MEDTRONIC INDONESIAAR Address
Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda
Registration Date
Sep 06, 2020
Expiry Date
Mar 12, 2025
Product Type
Surgical Neurology Equipment
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