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RANDOX Ransel Control - Indonesia BPOM Medical Device Registration

RANDOX Ransel Control is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101520238. The device is manufactured by RANDOX LABORATORIES LIMITED from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. CEKINDO BUSINESS INTERNATIONAL.

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
RANDOX Ransel Control
Analysis ID: AKL 20101520238

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United Kingdom

Authorized Representative

PT. CEKINDO BUSINESS INTERNATIONAL

AR Address

Gedung Axa Tower Lantai 36, Jalan Profesor Doktor Satrio Kaveling 18

Registration Date

Feb 03, 2025

Expiry Date

Nov 08, 2028

Product Type

Clinical Chemistry Test System

Quality control material (assayed and unassayed) (cair)

Invitro Diagnostics

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