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INNODX FT3 CMIA - Indonesia BPOM Medical Device Registration

INNODX FT3 CMIA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101421434. The device is manufactured by XIAMEN INNODX BIOTECH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SUMIFIN CITRA ABADI.

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
INNODX FT3 CMIA
Analysis ID: AKL 20101421434

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

SUMIFIN CITRA ABADI

AR Address

Jl. Alam Sutera Boulevard Alam Sutera Town Center (ASTC) Blok 10D No.19, Kel. Pakulonan, Kec. Serpong Utara - Tangerang Selatan 15325

Registration Date

Jul 29, 2024

Expiry Date

Feb 21, 2028

Product Type

Clinical Chemistry Test System

Total triiodothyronine test system (kit & cair)

Invitro Diagnostics

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