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Urit D31 Diluent - Indonesia BPOM Medical Device Registration

Urit D31 Diluent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208420246. The device is manufactured by URIT MEDICAL ELECTRONIC CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is INTIGLOBAL PERFECT RESULT SOURCE.

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
Urit D31 Diluent
Analysis ID: AKL 20208420246

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

INTIGLOBAL PERFECT RESULT SOURCE

AR Address

KOMPLEK DARMO PARK II BLOK 4/14

Registration Date

Sep 12, 2024

Expiry Date

Dec 31, 2026

Product Type

Hematological Reagents

Blood cell diluents

Invitro Diagnostics

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