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EUDAMED last updated this device on May 29, 2026
426059553MP23OSD01YUopticol® GL OSD is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by Penta Arzneimittel GmbH. Placed on the EU market in Portugal. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
14260595531874410998001 packaging level registered — each level carries its own UDI-DI.
14260595531874× 1 unitBase unit44260595531875× 1 unit(01)14260595531874
European Medical Device Nomenclature — the EU product classification assigned to this device.
Q02030301OPHTHALMOLOGY, HYALURONIC ACID AND DERIVATIVES12 warnings recorded — scroll inside the panel to see all entries.
Do not use the product if the safety ring of the tamper evident closure is broken or the bottle is damaged.
Do not use the eye drops beyond the expiry date which you can find on each multi-dose container and on the folding box.
Consult instructions for use.
If you also use other eye drops / eye ointment, wait about 15 minutes. These eye drops should always be used last.
OTHER
Primary placement in Portugal; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| PortugalPrimary placement | — | Still on market |
DE-MF-000006565The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Please keep the product out of reach of children.
Do not use in infected or injured eyes.
Do not touch the eye with the dropper.
Do not use if you are allergic to any of the ingredients.
In very rare cases, the use of the eye drops may cause irritation in very sensitive eyes or eye lids. The following eye disorders may occur: redness, pain, burning, stinging, itching, swelling, foreign body sensation.
Temporary blurring for a brief period may be experienced after application; avoid driving, operating machinery and wait until normal vision is restored.
In case a serious incident has occurred during the use of this medical device or as a result of its use, please report it to the manufacturer and the competent authority.
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.
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.