Pure Global

MEDONIC M51-D Diluent - Indonesia BPOM Medical Device Registration

MEDONIC M51-D Diluent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208912334. The device is manufactured by BOULE MEDICAL. from Sweden, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MRK DIAGNOSTICS.

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
MEDONIC M51-D Diluent
Analysis ID: AKL 20208912334

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

BOULE MEDICAL.

Country of Origin

Sweden

Authorized Representative

MRK DIAGNOSTICS

AR Address

JL. Merpati Mas I Blok B1 NO.46 Perkantoran Tanjung Mas Raya Tanjung Barat

Registration Date

Dec 17, 2023

Expiry Date

Dec 31, 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