Pure Global

COULTER Body Fluid Control - Indonesia BPOM Medical Device Registration

COULTER Body Fluid Control is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208220305. The device is manufactured by BECKMAN COULTER, INC (FLORIDA) from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DHH TRADING 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
COULTER Body Fluid Control
Analysis ID: AKL 20208220305

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. DHH TRADING INDONESIA

AR Address

Gedung World Trade Center 3, Lt. 20, Jl. Jend. Sudirman Kav. 29-31, Kel. Karet, Kec. Setiabudi, Jakarta Selatan, DKI Jakarta

Registration Date

Dec 15, 2023

Expiry Date

Feb 10, 2026

Product Type

Hematological Reagents

Hematology quality control mixture.

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from BECKMAN COULTER, INC (FLORIDA)
Products from the same manufacturer (1 products)