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EUDAMED last updated this device on Jul 23, 2025
805228659EIKT00010xxx5AFiber Optic for PLA Short (Red) is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by ELESTA SpA. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
08052286590319EI KT0 0010 310(01)08052286590319
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z12011080LASER SURGERY INSTRUMENTS - HARDWARE ACCESSORIES4 warnings recorded — scroll inside the panel to see all entries.
CW010CW009CW007CW001IT-MF-000037909IT343885The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Primary placement in Italy; available across 4 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | — | Still on market |
| Germany | — | Still on market |
| Spain | — | Still on market |
| France | — | 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 →Certificate health across this manufacturer's portfolio.
IT343885IssuedNotified 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 →805228659EIKT00010xxx5AOn the marketFiber Optic for PLA Short (Blue)805228659EIKT00010xxx5AOn the marketFiber Optic for PLA Short (Green)805228659EIKT00010xxx5AOn the marketFiber Optic for PLA Short (Yellow)805228659EIKT00010xxx5AOn the marketGROOVE805228659EIGU20008xxx4YOn the marketINFIX805228659EIGU20008xxx4YOn the market