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TOX A/B QUIK CHEK - Indonesia BPOM Medical Device Registration

TOX A/B QUIK CHEK is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208220167. The device is manufactured by TECHLAB INC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SCIENCEWERKE.

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 : B
TOX A/B QUIK CHEK
Analysis ID: AKL 20208220167

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

TECHLAB INC

Country of Origin

United States

Authorized Representative

PT. SCIENCEWERKE

AR Address

Jl.Palmerah Barat No.25

Registration Date

Jul 05, 2024

Expiry Date

May 08, 2027

Product Type

Hematological Reagents

Hematology quality control mixture.

Invitro Diagnostics

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