Pure Global

NODFORD Follicle-stimulating Hormone/ FSH (CLIA) Kit - Indonesia BPOM Medical Device Registration

NODFORD Follicle-stimulating Hormone/ FSH (CLIA) Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101422375. 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 PT. 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
NODFORD Follicle-stimulating Hormone/ FSH (CLIA) Kit
Analysis ID: AKL 20101422375

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. MEDQUEST GLOBAL PARTNERS

AR Address

Menara Salemba Lantai 7 zona 2 Jalan Salemba Raya Kav. 5 - 5A Jakarta Pusat 10440

Registration Date

Nov 18, 2024

Expiry Date

Oct 25, 2026

Product Type

Clinical Chemistry Test System

Follicle-stimulating hormone test system (kit & cair)

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing