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AMS Auto 3-part Hematology Analyzer - Indonesia BPOM Medical Device Registration

AMS Auto 3-part Hematology Analyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20205912910. The device is manufactured by WHEISMAN MEDICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TIRTA PASIFIK MEDIKATAMA.

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
AMS Auto 3-part Hematology Analyzer
Analysis ID: AKL 20205912910

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. TIRTA PASIFIK MEDIKATAMA

AR Address

JL. Jatibening Raya II, Ruko Jatibening No. 2 RT/RW 03/01

Registration Date

May 11, 2022

Expiry Date

May 11, 2025

Product Type

Automatic and Semi-Automatic Hematology Equipment

Automated cell counter.

Invitro Diagnostics

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DJ Fang

DJ Fang

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