- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on May 5, 2026
B-100012893UDERMATOP HEALING CREAM PLUS is an MDD-legacy medical device registered in EUDAMED. It is classified as Class III. Manufactured by Fidia Farmaceutici S.p.A.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
D-100012893U10001289D-100012893U
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA / IFA support is coming.
European Medical Device Nomenclature — the EU product classification assigned to this device.
M040499DRESSINGS FOR WOUNDS, SORES AND ULCERATIONS - OTHER9 warnings recorded — scroll inside the panel to see all entries.
OTHER
OTHER
OTHER
OTHER
OTHER
Primary placement in Germany; available across 3 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | — | Dec 31, 2027 |
| Czechia | — | Dec 31, 2027 |
| Slovakia | — | Dec 31, 2027 |
IT-MF-0000269882114366TE0135326OTHER
OTHER
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 →80336618004030200000000R5On the marketCONTACTA SOLLIEVO LENTI80336618004170100000000VFOn the marketCONTACTA SOLLIEVO LENTI80336618004170100000000VFOn the marketDERMATOP patch HI TECHB-100011502UOn the marketDERMATOP patch HI TECHB-100013022TOn the marketDUOGRAFTER II80336618005030100000000RPOn the marketNo certificate specifically references this device's Basic UDI-DI.
Certificate health across this manufacturer's portfolio.
067/MDRSupplemented40052SupplementedNotified 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 →