Pure Global

BDI Lab Lyte Electrolyte Analyzer and Accessories - Indonesia BPOM Medical Device Registration

BDI Lab Lyte Electrolyte Analyzer and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102220011. The device is manufactured by DIAMOND DIAGNOSTICS, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BERLIANTAMA DIAGNOSTIKA 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
BDI Lab Lyte Electrolyte Analyzer and Accessories
Analysis ID: AKL 20102220011

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. BERLIANTAMA DIAGNOSTIKA INDONESIA

AR Address

JL.TAMAN SUNTER INDAH BLOK HJ2 NO.16

Registration Date

Jan 18, 2022

Expiry Date

Jan 14, 2025

Product Type

Clinical Laboratory Equipment

Electrolyte analyzer

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing