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Yumizen CR UREA/BUN (UV) - Indonesia BPOM Medical Device Registration

Yumizen CR UREA/BUN (UV) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101421965. The device is manufactured by HORIBA INDIA PRIVATE LIMITED from India, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is 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.

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BPOM Registered
Risk Class Kelas Resiko : B
Yumizen CR UREA/BUN (UV)
Analysis ID: AKL 20101421965

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

HORIBA INDONESIA

AR Address

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

Registration Date

Oct 07, 2024

Expiry Date

Feb 26, 2029

Product Type

Clinical Chemistry Test System

Urea nitrogen test system (kit & cair)

Invitro Diagnostics

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