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AIM Filter - Indonesia BPOM Medical Device Registration

AIM Filter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10203025904. The device is manufactured by GUANGZHOU LEIDE BIOSCIENCES CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. 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 : A
AIM Filter
Analysis ID: AKL 10203025904

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

FOKUS DIAGNOSTIC INDONESIA

AR Address

Komp. Majapahit Permai Blok B No. 118 Jl. Majapahit Raya

Registration Date

Oct 06, 2020

Expiry Date

Dec 31, 2023

Product Type

Pathology Equipment and Accessories

Specimen transport and storage container.

Invitro Diagnostics

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