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WILAflow Elite Non Invasive Ventilator - Indonesia BPOM Medical Device Registration

WILAflow Elite Non Invasive Ventilator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403716990. The device is manufactured by WILAMED GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is MULTIPURPOSE CIPTASENTOSA.

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
WILAflow Elite Non Invasive Ventilator
Analysis ID: AKL 20403716990

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

WILAMED GMBH

Country of Origin

Germany

Authorized Representative

MULTIPURPOSE CIPTASENTOSA

AR Address

Surapati Core Blok M No.1 Jl. Phh. Mustofa No. 39 Bandung 022-87241400

Registration Date

Jul 26, 2023

Expiry Date

May 04, 2026

Product Type

Therapeutic Anesthesia Equipment

Noncontinuous ventilator (IPPB).

Non Radiation Electromedics

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