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IMPROVE Auto ESR Analyzer - Indonesia BPOM Medical Device Registration

IMPROVE Auto ESR Analyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10205420012. The device is manufactured by CARETIUM MEDICAL INSTRUMENTS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. 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 : A
IMPROVE Auto ESR Analyzer
Analysis ID: AKL 10205420012

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. MACROCITRA ARDANASEJATI

AR Address

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

Registration Date

Jan 11, 2024

Expiry Date

Jul 02, 2028

Product Type

Automatic and Semi-Automatic Hematology Equipment

Automated sedimentation rate device.

Invitro Diagnostics

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