Pure Global

Adiag Hematology Diluent W-61D - Indonesia BPOM Medical Device Registration

Adiag Hematology Diluent W-61D is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208320860. The device is manufactured by WHEISMAN MEDICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ALIZAH.

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
Adiag Hematology Diluent W-61D
Analysis ID: AKL 20208320860

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. ALIZAH

AR Address

JL. OTISTA III NO.10A RT 001 RW 004 KEL.CIPINANG CEMPEDAK KEC.JATINEGARA

Registration Date

Nov 24, 2023

Expiry Date

Nov 23, 2026

Product Type

Hematological Reagents

Blood cell diluents

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing