- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on May 28, 2026
80232790000A03996200110DSTUBO SILICONE 12x18mm - spess. 3 mm is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by GIMA SPA. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0802327925485325485(01)08023279254853
European Medical Device Nomenclature — the EU product classification assigned to this device.
A0399TUBULAR DEVICES - OTHER1 warning recorded — scroll inside the panel to see all entries.
IT-MF-000011004The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Primary placement in Italy; available across 5 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | — | Still on market |
| France | — | Still on market |
| Hungary | — | Still on market |
| Romania | — | Still on market |
| Slovakia | — | Still on market |
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.
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 →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 →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 →No certificate specifically references this device's Basic UDI-DI.
80232790000A03996200110DSOn the marketTUBO SILICONE 10x16mm - spess. 3 mm80232790000A03996200110DSOn the marketTUBO SILICONE 10x20mm - spess. 5 mm80232790000A03996200110DSOn the marketTUBO SILICONE 1x3mm - spess. 1 mm80232790000A03996200110DSOn the marketTUBO SILICONE 2x4mm - spess. 1 mm80232790000A03996200110DSOn the marketTUBO SILICONE 3x5mm - spess. 1 mm80232790000A03996200110DSOn the marketCertificate health across this manufacturer's portfolio.
IT349382IssuedIT349382IssuedNotified 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 →