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LumiraDx INR Quality Control - Indonesia BPOM Medical Device Registration

LumiraDx INR Quality Control is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101220302. The device is manufactured by HART BIOLOGICAL LTD from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MEDQUEST GLOBAL PARTNERS.

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
LumiraDx INR Quality Control
Analysis ID: AKL 20101220302

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United Kingdom

Authorized Representative

MEDQUEST GLOBAL PARTNERS

AR Address

MENARA SALEMBA LANTAI 7, JALAN SALEMBA RAYA NOMOR 5-5A

Registration Date

Jun 06, 2023

Expiry Date

Jan 01, 2028

Product Type

Clinical Chemistry Test System

Quality control material (assayed and unassayed) (cair)

Invitro Diagnostics

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