PERIMED PeriFlux 6000 Combined System - Indonesia BPOM Medical Device Registration
PERIMED PeriFlux 6000 Combined System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502220378. The device is manufactured by PERIMED AB. SWEDEN from Sweden, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INDOMED KAHANASTI INDONESIA.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
PERIMED AB. SWEDENCountry of Origin
Sweden
Authorized Representative
PT. INDOMED KAHANASTI INDONESIAAR Address
Grand Centro Bintaro Blok B, Jalan Kodam Bintaro No.5A RT/RW.005/003 Kel. Pesanggrahan, Kec. Pesanggrahan, Jakarta Selatan. Telp. (021) 2270
Registration Date
Nov 17, 2022
Expiry Date
May 10, 2024
Product Type
Monitoring Cardiology Equipment
Cardiovascular blood flowmeter.
Non Radiation Electromedics
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