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EUDAMED last updated this device on Aug 7, 2026
4250274711211SVIP113316F1 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 France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
DE-MF-000005284G70 107055 0007(01)04250274706399
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 France; available across 11 countries total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Dec 17, 2025 | Still on market |
| Austria | May 12, 2026 | Still on market |
| Belgium | Jun 17, 2026 | Still on market |
| Czechia | Jan 19, 2026 | Still on market |
| Denmark | Jun 30, 2026 | Still on market |
| Finland | Jun 30, 2026 | Still on market |
| Italy | Mar 5, 2026 | Still on market |
| Luxembourg | Jun 17, 2026 | Still on market |
| Latvia | May 5, 2026 | Still on market |
| Netherlands | Jun 17, 2026 | Still on market |
| Sweden | Jun 30, 2026 | Still on market |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
04250274706399Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
4250274711211SVIP113316F1UDI 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.
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 →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 →