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ClearLLab 10C T Cell Tube - Indonesia BPOM Medical Device Registration

ClearLLab 10C T Cell Tube is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207320377. The device is manufactured by BECKMAN COULTER INDIA PRIVATE LIMITED. from India, and is classified as Risk Class Kelas Resiko : C. 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.

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BPOM Registered
Risk Class Kelas Resiko : C
ClearLLab 10C T Cell Tube
Analysis ID: AKL 20207320377

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

India

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

Aug 15, 2023

Expiry Date

Jun 01, 2025

Product Type

Haematology Package and Kit

Flow cytometric test system for hematopoietic neoplasms

Invitro Diagnostics

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DJ Fang

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