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VARIFIT™ NIV Non-Vented Mask - Indonesia BPOM Medical Device Registration

VARIFIT™ NIV Non-Vented Mask is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403818891. The device is manufactured by SLEEPNET CORPORATION from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MADESA SEJAHTERA UTAMA.

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 : C
VARIFIT™ NIV Non-Vented Mask
Analysis ID: AKL 20403818891

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. MADESA SEJAHTERA UTAMA

AR Address

JL. GUNUNG SAHARI RAYA 51- A NO.14

Registration Date

Jun 26, 2021

Expiry Date

Mar 10, 2024

Product Type

Therapeutic Anesthesia Equipment

Noncontinuous ventilator (IPPB).

Non Electromedic Non Sterile

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