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FEROZE Probe Cleaner - Indonesia BPOM Medical Device Registration

FEROZE Probe Cleaner is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204420252. The device is manufactured by URIT MEDICAL ELECTRONIC CO., LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BUANA INTIPRIMA MEDIKA.

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
FEROZE Probe Cleaner
Analysis ID: AKL 10204420252

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. BUANA INTIPRIMA MEDIKA

AR Address

Rukan Sentra Niaga Green Lake City Blok F No.3

Registration Date

Oct 18, 2024

Expiry Date

Oct 16, 2027

Product Type

Reagents and Specimen Providers

General purpose reagent.

Invitro Diagnostics

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