- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Sep 10, 2026
B-+D945PEG3000250Impact Repair; pink veined; 500 g is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by retec Kunststofftechnik GmbH. Placed on the EU market in Hungary. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
+D945PEG3000250300025+D945PEG3000250
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.
Q010699MATERIALS FOR THE PREPARATION OF CUSTOM-MADE DENTAL DEVICES - OTHER4 warnings recorded — scroll inside the panel to see all entries.
dibenzoyl peroxide; benzoyl peroxide
DE-MF-000000086059034 MR2Primary placement in Hungary; available across 3 countries total.
| Country | On market since | Until |
|---|---|---|
| HungaryPrimary placement | — | Still on market |
| Spain | — | Still on market |
| Portugal | — | 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 →No certificate specifically references this device's Basic UDI-DI.
B-+D945PEG3000100On the marketImpact Repair; dark pink; 500 g;B-+D945PEG3000150On the marketImpact Repair; pink veined; 1000 gB-+D945PEG3000200On the marketSELACRYL COLD; colorless, 1 LB-+D945SX9589160On the marketSELACRYL COLD; colorless, 500 mlB-+D945SX9589100On the marketSELACRYL COLD; pink V, 1 kgB-+D945SX9589090On 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.