Pure Global

REDCELL CELL SCREEN 1-2-3 - Indonesia BPOM Medical Device Registration

REDCELL CELL SCREEN 1-2-3 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209027020. The device is manufactured by RED CELL BIYOTEKNOLOJI A.S, from Turkey, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PANJI PRIMA DINAMIKA.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
REDCELL CELL SCREEN 1-2-3
Analysis ID: AKL 20209027020

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Turkey

Authorized Representative

PT. PANJI PRIMA DINAMIKA

AR Address

Jalan Kalibata Timur III No. 55 Kalibata, Pancoran

Registration Date

Nov 17, 2020

Expiry Date

Dec 30, 2025

Product Type

Products used in the manufacture of blood preparations and preparations of origin and blood

Automated blood grouping and antibody test system.

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing