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EUDAMED last updated this device on Jun 3, 2026
B-06974624060044Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →N/A is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by Wuhan Pioon Technology Co., Ltd. Placed on the EU market in Spain. 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 →06974624060044Basic 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 →B-06974624060044N/AUDI 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)06974624060044
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z12011016DIODE SURGICAL LASERSterile
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.
Primary placement in Spain; available across 9 countries total.
| Country | On market since | Until |
|---|---|---|
| SpainPrimary placement | Apr 10, 2020 | Feb 28, 2024 |
| France | May 25, 2020 | Jan 25, 2022 |
| Hungary | Apr 22, 2020 | Mar 12, 2026 |
| Italy | Aug 26, 2021 | Mar 17, 2026 |
| Lithuania | Jun 9, 2020 | Oct 27, 2021 |
| Luxembourg | Jan 27, 2021 | Jan 28, 2021 |
| Poland | Sep 29, 2020 | Mar 11, 2026 |
| Romania | Aug 25, 2020 | Mar 28, 2022 |
| Türkiye | Aug 28, 2020 | Dec 17, 2021 |
CN-MF-000018399No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.G1 097889 0004