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AltaGel S Blood Group Card Centrifuge - Indonesia BPOM Medical Device Registration

AltaGel S Blood Group Card Centrifuge is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10209320660. The device is manufactured by AIKANG MEDTECH CO., LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. FAITHFUL MEDICAL GRACE.

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 : A
AltaGel S Blood Group Card Centrifuge
Analysis ID: AKL 10209320660

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. FAITHFUL MEDICAL GRACE

AR Address

Mitra Sunter Boulevard Blok B No.39 Jl. Yos Sudarso Kav. 89

Registration Date

Oct 04, 2023

Expiry Date

Feb 02, 2026

Product Type

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

Blood bank centrifuge for in vitro diagnostic use.

Invitro Diagnostics

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