- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Oct 24, 2025
B-08017990085773Pic solution - pansements ampoules talons is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Eurosirel Spa. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
08017990085773IA085773(01)08017990085773
European Medical Device Nomenclature — the EU product classification assigned to this device.
M0599MEDICAL PLASTERS - OTHERIT-MF-0000059821648/MDDPrimary placement in France; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | — | 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.
293/MDRIssuedCVD005826IssuedCSQ0031250126SupplementedNotified 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 →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.
8017990PCLH6On the marketPic solution - Pansements ampoules mix 3 taillesB-08017990085797On the marketPic solution - pansements ampoules orteilsB-08017990085780On the marketPICA Italia 40 Cerotti classici8017990CMYGVOn the marketPingo doce - pensos ovais para calos8017990PCFGSOn the marketPingo doce - Pensos para calos8017990PCEGQOn the market