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EUDAMED last updated this device on May 7, 2026
7331791-HME-0-000-0001-XCProvox Life Go HME Experience is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Atos Medical AB. Placed on the EU market in Belgium. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0733179101611082651 packaging level registered — each level carries its own UDI-DI.
07331791016110× 1 unitBase unit07331791017490× 50 unitsSE-MF-000000725(01)07331791016110
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
Primary placement in Belgium; available across 8 countries total.
| Country | On market since | Until |
|---|---|---|
| BelgiumPrimary placement | — | Still on market |
| Denmark | — | Still on market |
| Finland | — | Still on market |
| France | — | Still on market |
| Luxembourg | — | Still on market |
| Netherlands | — | Still on market |
| Norway | — | Still on market |
| Sweden | — | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
R060299HUMIDIFICATION SYSTEMS - OTHERPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →MDR risk classes
MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →7331791-HME-0-000-0007-XWOn the marketProvox Life FreeHands HME7331791-HME-0-000-0008-XZOn the marketProvox Life Go HME7331791-HME-0-000-0001-XCOn the marketProvox Life Home HME7331791-HME-0-000-0001-XCOn the marketProvox Life Home HME Experience7331791-HME-0-000-0001-XCOn the marketProvox Life Night HME7331791-HME-0-000-0001-XCOn the marketNo certificate specifically references this device's Basic UDI-DI.
Certificate health across this manufacturer's portfolio.
C520850IssuedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →