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MANI H FILES - Indonesia BPOM Medical Device Registration

MANI H FILES is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10603023662. The device is manufactured by MANI HANOI CO. LTD. PHO YEN FACTORY from Vietnam, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. FIXIPRIMA PERSADA.

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
MANI H FILES
Analysis ID: AKL 10603023662

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Vietnam

Authorized Representative

PT. FIXIPRIMA PERSADA

AR Address

Jl. Pintu Air Raya No. 7, Blok B-5 Jakarta

Registration Date

Sep 15, 2021

Expiry Date

Aug 31, 2025

Product Type

Surgical Dental Equipment

Dental hand instrument

Non Electromedic Non Sterile

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