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EUDAMED last updated this device on Dec 29, 2025
B-DE-MF-000025076FPDontodent Intensiv Gebissreiniger is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by Propack Produkte für Haushalt und Körperpflege GmbH. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
DE-MF-00002507610000368846-Product Assurance-NA-DNKD-DE-MF-000025076FP
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA / IFA support is coming.
1 warning recorded — scroll inside the panel to see all entries.
Enthält Potassium Caroate und Eukalyptol
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.
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.
Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
Primary placement in Germany; available across 7 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Nov 1, 2024 | Still on market |
| Austria | Nov 1, 2024 | Still on market |
| Bulgaria | Jul 3, 2025 | Still on market |
| Hungary | Jun 23, 2025 | Still on market |
| Italy | Jan 14, 2025 | Still on market |
| Poland | May 19, 2025 | Still on market |
| Slovakia | Apr 23, 2025 | Still on market |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
D-DE-MF-000025076FPBasic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
B-DE-MF-000025076FPSKU 3304881UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
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.
European Medical Device Nomenclature — the EU product classification assigned to this device.
V0799PRODUCTS FOR CLEANING MEDICAL DEVICES NOT INCLUDED IN OTHER CLASSES - OTHERPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →B-04001245969509A4On the marketDontodent Intensiv GebissreinigerB-040012450035863MOn the marketDontodent Intensiv GebissreinigerB-0400124500356237On the marketDontodent Super Haftcreme GeschmacksneutralB-0400124500434738On the marketDontodent ZahnspangenreinigerB-040012450035312UOn the marketNo 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.