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CARETRIS Glucometer - Indonesia BPOM Medical Device Registration

CARETRIS Glucometer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101421064. The device is manufactured by SEJOY BIOMEDICAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TRISA LIKUID FARMA.

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
CARETRIS Glucometer
Analysis ID: AKL 20101421064

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. TRISA LIKUID FARMA

AR Address

PERUM GAYAMSARI BLOK B. 28/29 RT01/011

Registration Date

Aug 26, 2024

Expiry Date

Jun 03, 2027

Product Type

Clinical Chemistry Test System

Glucose test system

Invitro Diagnostics

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