- Organization name
- UDI-DI code
- Reference / catalog number
CN-MF-000007053544291 MRANumen is an MDD-legacy medical device registered in EUDAMED. It is classified as Class III. Manufactured by MicroPort NeuroTech (Shanghai) Co.,Ltd.. Placed on the EU market in Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Aug 6, 2024
B-06958698015230Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)06958698015230
5 warnings recorded — scroll inside the panel to see all entries.
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 Spain; available across 13 countries total.
| Country | On market since | Until |
|---|---|---|
| SpainPrimary placement | Aug 1, 2021 | Dec 31, 2027 |
| Belgium | Nov 1, 2023 | Dec 31, 2027 |
| Germany | Sep 1, 2023 | Dec 31, 2027 |
| EL | Aug 1, 2023 | Dec 31, 2027 |
| France | Apr 1, 2024 | Dec 31, 2027 |
| Croatia | Jan 1, 2023 | Dec 31, 2027 |
| Ireland | Apr 1, 2023 | Dec 31, 2027 |
| Italy | Jul 1, 2023 | Dec 31, 2027 |
| Netherlands | Nov 1, 2022 | Dec 31, 2027 |
| Poland | Jun 1, 2022 | Dec 31, 2027 |
| Portugal | Aug 1, 2021 | Dec 31, 2027 |
| Romania | Jan 1, 2024 | Dec 31, 2027 |
| XI | Dec 1, 2023 | Dec 31, 2027 |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
06958698015230Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
B-069586980152303D0625FRUDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
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.
European Medical Device Nomenclature — the EU product classification assigned to this device.
C010402020301EMBOLISATION COILSCertificate health across this manufacturer's portfolio.
1000324357Issued1000323760Supplemented1000316127Supplemented1000245870IssuedNotified 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 →Notified 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 →Notified 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 →Notified 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 →No certificate specifically references this device's Basic UDI-DI.