MyCells Autologous Platelet Preparation Kit - Indonesia BPOM Medical Device Registration
MyCells Autologous Platelet Preparation Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10102220366. The device is manufactured by PRO-TECH DESIGN & MFG, INC from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PRIMA CENTER MEDIKACITRA.
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 : 1
Manufacturer
PRO-TECH DESIGN & MFG, INCCountry of Origin
United States
Authorized Representative
PRIMA CENTER MEDIKACITRAAR Address
Jl. Paseban Raya No. 21 Salemba
Registration Date
Dec 26, 2022
Expiry Date
Sep 07, 2025
Product Type
Clinical Laboratory Equipment
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