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NODFORD Dry Fluorescence Immunoassay Analyzer - Indonesia BPOM Medical Device Registration

NODFORD Dry Fluorescence Immunoassay Analyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20304420040. The device is manufactured by SHENZHEN NODFORD INDUSTRIAL CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MULTISERA INDOSA.

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
NODFORD Dry Fluorescence Immunoassay Analyzer
Analysis ID: AKL 20304420040

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

MULTISERA INDOSA

AR Address

Jl. Jend. Sudirman No. 689 RT/RW : 21/07

Registration Date

May 20, 2024

Expiry Date

Nov 09, 2026

Product Type

Immunology Laboratory Equipment and Reagents

Immunofluorometer equipment

Invitro Diagnostics

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DJ Fang

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