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MEDIN NUFLOW Nasal Cannula Set - Indonesia BPOM Medical Device Registration

MEDIN NUFLOW Nasal Cannula Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403910958. The device is manufactured by MEDIN MEDICAL INNOVATIONS GMBH. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. AMPM HEALTHCARE 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
MEDIN NUFLOW Nasal Cannula Set
Analysis ID: AKL 10403910958

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

PT. AMPM HEALTHCARE INDONESIA

AR Address

Jl.Cengkeh Kav.16 No.29-30

Registration Date

Sep 24, 2020

Expiry Date

Jun 23, 2025

Product Type

Therapeutic Anesthesia Equipment

Nasal oxygen cannula.

Non Electromedic Non Sterile

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