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ConfiCare M1 Multi Analyzer - Indonesia BPOM Medical Device Registration

ConfiCare M1 Multi Analyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10102420214. The device is manufactured by CAREFORU. CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. GENBODY INDONESIA SEJAHTERA.

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
ConfiCare M1 Multi Analyzer
Analysis ID: AKL 10102420214

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

CAREFORU. CO., LTD

Country of Origin

Korea

Authorized Representative

PT. GENBODY INDONESIA SEJAHTERA

AR Address

Jl. A. Yani 221-223 Ruko Segitiga Mas Kav. H-6

Registration Date

Jul 31, 2024

Expiry Date

May 09, 2029

Product Type

Clinical Laboratory Equipment

Colorimeter, photometer, or spectrophotometer for clinical use.

Invitro Diagnostics

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