Pure Global

ClearLLab Control Cells Abnormal - Indonesia BPOM Medical Device Registration

ClearLLab Control Cells Abnormal is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208320682. The device is manufactured by DASH, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is FOKUS DIAGNOSTIC 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
ClearLLab Control Cells Abnormal
Analysis ID: AKL 20208320682

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

DASH, INC.

Country of Origin

United States

Authorized Representative

FOKUS DIAGNOSTIC INDONESIA

AR Address

Jl. Jatipadang Raya No.9A, RT.6/RW.4, Kelurahan Jatipadang, Kecamatan Pasar Minggu, Kota Jakarta Selatan, DKI Jakarta 12540

Registration Date

Feb 06, 2025

Expiry Date

Dec 31, 2027

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