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MERILYZER CelQuant 3i™ - Indonesia BPOM Medical Device Registration

MERILYZER CelQuant 3i™ is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20205512553. The device is manufactured by MERIL DIAGNOSTICS PVT., LTD. from India, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MSR GREEN LESTARI.

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
MERILYZER CelQuant 3i™
Analysis ID: AKL 20205512553

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

MSR GREEN LESTARI

AR Address

Jl. Agung Utara I A2 - 27 Sunter Agung Podomoro. Telp : 021-65307518

Registration Date

Dec 14, 2023

Expiry Date

Nov 09, 2026

Product Type

Automatic and Semi-Automatic Hematology Equipment

Automated differential cell counter

Invitro Diagnostics

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