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IMPROVACUTER ESR Plastic Tubes - Indonesia BPOM Medical Device Registration

IMPROVACUTER ESR Plastic Tubes is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101913512. The device is manufactured by GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MACROCITRA ARDANASEJATI.

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
IMPROVACUTER ESR Plastic Tubes
Analysis ID: AKL 20101913512

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

MACROCITRA ARDANASEJATI

AR Address

Rukan Taman Meruya Blok M-65 Meruya Ilir - Jakarta Barat Telp. 021-5874575, Fax. 021-5874573

Registration Date

Oct 04, 2023

Expiry Date

Jul 02, 2028

Product Type

Clinical Chemistry Test System

Blood specimen collection device

Invitro Diagnostics

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