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EUDAMED last updated this device on Apr 8, 2026
8719327092NWMJZPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →NA is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by LivAssured B.V.. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
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 →08719327236079Basic 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 →8719327092NWMJZNAUDI 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 →(01)08719327236079
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
European Medical Device Nomenclature — the EU product classification assigned to this device.
V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHERSterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
View in glossary →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.
View in glossary →Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
View in glossary →CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
View in glossary →Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
View in glossary →No certificate specifically references this device's Basic UDI-DI.
This device is not currently linked to any other device.
Primary placement in Netherlands; available across 31 countries total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | May 1, 2025 | Still on market |
| Austria | May 1, 2025 | Still on market |
| Belgium | May 1, 2025 | Still on market |
| Bulgaria | Aug 28, 2025 | Still on market |
| Cyprus | Dec 4, 2025 | Still on market |
| Czechia | Jul 15, 2025 | Still on market |
| Germany | May 1, 2025 | Still on market |
| Denmark | May 1, 2025 | Still on market |
| Estonia | Nov 11, 2025 | Still on market |
| EL | Dec 4, 2025 | Still on market |
| Spain | May 1, 2025 | Still on market |
| Finland | Jun 10, 2025 | Still on market |
| France | May 1, 2025 | Still on market |
| Croatia | Mar 25, 2026 | Still on market |
| Hungary | Mar 5, 2026 | Still on market |
| Ireland | May 1, 2025 | Still on market |
| Iceland | May 31, 2025 | Still on market |
| Italy | May 1, 2025 | Still on market |
| Liechtenstein | May 1, 2025 | Still on market |
| Lithuania | Dec 4, 2025 | Still on market |
| Luxembourg | May 1, 2025 | Still on market |
| Latvia | Jan 31, 2026 | Still on market |
| Malta | Jan 31, 2026 | Still on market |
| Norway | May 23, 2025 | Still on market |
| Poland | May 23, 2025 | Still on market |
| Portugal | Dec 9, 2025 | Still on market |
| Romania | Jan 21, 2026 | Still on market |
| Sweden | May 23, 2025 | Still on market |
| Slovakia | Jun 17, 2025 | Still on market |
| Türkiye | Jan 15, 2026 | Still on market |
| XI | May 1, 2025 | Still on market |
NL-MF-000022904Certificate health across this manufacturer's portfolio.
MDR-0027IssuedNotified 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 →