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EUDAMED last updated this device on Jun 22, 2026
8588009045OCUflashblueLMOCUflash® blue Augentropfen, Lösung is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by Unimed Pharma spol. s r.o.. Placed on the EU market in Austria. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
08588009045502591 packaging level registered — each level carries its own UDI-DI.
08588009045502× 1 unitBase unit28588009045506× 300 units(01)08588009045502
European Medical Device Nomenclature — the EU product classification assigned to this device.
Q02030299OPHTHALMOLOGY, LIQUID FLUIDS - OTHER1 warning recorded — scroll inside the panel to see all entries.
Primary placement in Austria; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| AustriaPrimary placement | Mar 31, 2026 | Still on market |
SK-MF-000003111The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
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.
8588009045OCUflash7KOn the marketOCUflash® akių lašai (tirpalas)8588009045OCUflash7KOn the marketOCUflash® Augentropfen, Lösung8588009045OCUflash7KOn the marketOCUflash® blue picături oftalmice, soluție8588009045OCUflashblueLMOn the marketOCUflash® blue acu pilieni, šķīdums8588009045OCUflashblueLMOn the marketOCUflash® blue akių lašai (tirpalas)8588009045OCUflashblueLMOn the marketNo certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.