- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Aug 11, 2026
4250274711111SQIP070012F3 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class III. Manufactured by FEG Textiltechnik Forschungs- und Entwicklungsgesellschaft mbH. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
04250274701066IP070012F3DE-MF-000005284G70 107055 0007(01)04250274701066
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
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 Italy; available across 7 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Jan 12, 2026 | Still on market |
| Belgium | Feb 19, 2026 | Still on market |
| Cyprus | Jan 20, 2026 | Still on market |
| EL | Jan 20, 2026 | Still on market |
| France | Jan 19, 2026 | Still on market |
| Luxembourg | Feb 19, 2026 | Still on market |
| Netherlands | Feb 19, 2026 | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
P900204SURGICAL MESHES, MORE THAN ONE COMPONENTPrimary 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 →Certificate health across this manufacturer's portfolio.
G15 107055 0012IssuedG70 107055 0007IssuedG70 107055 0006IssuedG70 107055 0005IssuedG70 107055 0003IssuedNotified 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 →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 →