LR-ACT - Indonesia BPOM Medical Device Registration
LR-ACT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207716296. The device is manufactured by MEDTRONIC PERFUSION SYSTEMS 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
MEDTRONIC PERFUSION SYSTEMSCountry of Origin
United States
Authorized Representative
PT. MEDTRONIC INDONESIAAR Address
Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda
Registration Date
Nov 06, 2020
Expiry Date
Apr 11, 2024
Product Type
Haematology Package and Kit
Activated whole blood clotting time tests.
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