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REDCELL LISS DILUENT - Indonesia BPOM Medical Device Registration

REDCELL LISS DILUENT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209024913. The device is manufactured by RED CELL BIYOKTEKNOLOJI A.S from Turkey, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is 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.

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BPOM Registered
Risk Class Kelas Resiko : C
REDCELL LISS DILUENT
Analysis ID: AKL 20209024913

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Turkey

Authorized Representative

PANJI PRIMA DINAMIKA

AR Address

Jalan Kalibata Timur III No. 55 Kalibata, Pancoran

Registration Date

Feb 06, 2025

Expiry Date

Dec 30, 2029

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

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