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REMI Serology Centrifuge - Indonesia BPOM Medical Device Registration

REMI Serology Centrifuge is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102420098. The device is manufactured by REMI ELEKTROTECHNIK LTD. from India, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DJUNIAR & DJUNIAR.

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 : B
REMI Serology Centrifuge
Analysis ID: AKL 20102420098

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

PT. DJUNIAR & DJUNIAR

AR Address

KOMPLEK RUKAN MAHKOTA ANCOL BLOK D NO.26,JLR.E MARTADINATA ,Desa/Kelurahan Pademangan Barat, Kec.Pademangan,Kota Adm.Jakarta Utara, Provinsi DKI Jakarta. Kode Pos:14420

Registration Date

Apr 05, 2024

Expiry Date

Dec 31, 2026

Product Type

Clinical Laboratory Equipment

Centrifugal chemistry analyzer for clinical use

Invitro Diagnostics

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