Pure Global

YUMIZEN G CTRL DDi I & II - Indonesia BPOM Medical Device Registration

YUMIZEN G CTRL DDi I & II is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208020453. The device is manufactured by DIAGON LTD from Hungary, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. HORIBA INDONESIA.

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
YUMIZEN G CTRL DDi I & II
Analysis ID: AKL 20208020453

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

DIAGON LTD

Country of Origin

Hungary

Authorized Representative

PT. HORIBA INDONESIA

AR Address

Jl. Jalur Sutera , Blok. 20A, No. 16 - 17, Kel. Kunciran, Kec. Pinang

Registration Date

Nov 26, 2024

Expiry Date

Nov 30, 2028

Product Type

Hematological Reagents

Hematology quality control mixture.

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing