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EUDAMED last updated this device on May 28, 2026
802327900M0501010000000MEROCCHETTO CEROTTO SETA 10 m x 5 cm 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.
0802327934788334788IT-MF-000011004(01)08023279347883
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
2 warnings recorded — scroll inside the panel to see all entries.
CW999CW009Sterile
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 | — | Still on market |
| Cyprus | — | Still on market |
| EL | — | Still on market |
| Spain | — | Still on market |
| France | — | Still on market |
| Luxembourg | — | Still on market |
| Portugal | — | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
M050101PLASTERS ON SPOOLS (ROLLS)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 →802327900R900902C400000LZOn the marketRIFLESSOLOGO802327900L1601014700000TGOn the marketROCCHETTO CEROTTO SETA 10 m x 2,5 cm802327900M0501010000000MEOn the marketRULLI DENTALI COTONE (10 scatole da 1.000)802327900Q0190040000000XROn the marketS/S I.V. STAND FOR BED - 4 hooks80232790000V90994500000C3On the marketSCALER - fig. 1802327900L1590994800000DUOn 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 →No certificate specifically references this device's Basic UDI-DI.