MI PISTOR 5 - Indonesia BPOM Medical Device Registration
MI PISTOR 5 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902323092. The device is manufactured by MI MEDICAL INNOVATION from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is REDO MARKETING 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
MI MEDICAL INNOVATIONCountry of Origin
France
Authorized Representative
REDO MARKETING INDONESIAAR Address
Ruko Renata Jl.Jalur Sutera Timur Blok 1A No. 9 Alam Sutera Kel. Kunciran Kec. Pinang
Registration Date
Dec 29, 2023
Expiry Date
Sep 15, 2028
Product Type
Therapeutic General and Individual Hospital Equipment
Piston syringe.
Non Radiation Electromedics

