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EUDAMED last updated this device on Nov 10, 2025
B-08699606684176POLİFLEKS is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Polifarma İlaç San. ve Tic. A.Ş.. Placed on the EU market in Türkiye. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0869960668417615000175(01)08699606684176
European Medical Device Nomenclature — the EU product classification assigned to this device.
A03040299IRRIGATION KITS, SINGLE-USE - OTHER1 warning recorded — scroll inside the panel to see all entries.
- Read the instructions for use before application. - Do not use if the solution is not clear, contains particles or package is damaged. - Microwave heating of the solution is not recommended. - Asepsis rules must be followed during application. - For single use. Do not use remaining solution. - After the package is opened, the solution should be used promptly to minimize the possibility of bacterial growth or pyrogen formation. - Do not used the product after its expiration date. - It should be used with caution in patients with heart failure and severe kidney failure. - Keep out of the reach and sight of children. - It should be used with caution in patients with hyperhydration, hypernatremia, and hyperchloremia.
Primary placement in Türkiye; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| TürkiyePrimary placement | — | Still on market |
TR-MF-000023645 1984-MDD-10-065Sterile
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.
No 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.