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EUDAMED last updated this device on Feb 11, 2026
69207567DNG0001GLPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Foley Catheter for single use [ latex Two-way with ballone) 4.7mm(14Fr)] is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Jiangxi Hongda Medical Equipment Group Ltd.. Placed on the EU market in Hungary. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
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 →06920756758373Basic 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 →69207567DNG0001GLFR14DUDI 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 →(01)06920756758373
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
European Medical Device Nomenclature — the EU product classification assigned to this device.
U020202URETERAL CATHETERS WITH FLUTE TIP WITH BALLOON3 warnings recorded — scroll inside the panel to see all entries.
CW010CW009CW007Sterile
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 →No certificate specifically references this device's Basic UDI-DI.
Primary placement in Hungary; available across 32 countries total.
| Country | On market since | Until |
|---|---|---|
| HungaryPrimary placement | Jan 1, 2020 | Jan 1, 2050 |
| Austria | Jan 1, 2020 | Jan 1, 2050 |
| Belgium | Jan 1, 2020 | Jan 1, 2050 |
| Bulgaria | Jan 1, 2020 | Jan 1, 2050 |
| Cyprus | Jan 1, 2020 | Jan 1, 2050 |
| Czechia | Jan 1, 2020 | Jan 1, 2050 |
| Germany | Jan 1, 2020 | Jan 1, 2050 |
| Denmark | Jan 1, 2020 | Jan 1, 2050 |
| Estonia | Jan 1, 2020 | Jan 1, 2050 |
| EL | Jan 1, 2020 | Jan 1, 2050 |
| Spain | Jan 1, 2020 | Jan 1, 2050 |
| Finland | Jan 1, 2020 | Jan 1, 2050 |
| France | Jan 1, 2020 | Jan 1, 2050 |
| Croatia | Jan 1, 2020 | Jan 1, 2050 |
| Ireland | Jan 1, 2020 | Jan 1, 2050 |
| Iceland | Jan 1, 2020 | Jan 1, 2050 |
| Italy | Jan 1, 2020 | Jan 1, 2050 |
| Liechtenstein | Jan 1, 2020 | Jan 1, 2050 |
| Lithuania | Jan 1, 2020 | Jan 1, 2050 |
| Luxembourg | Jan 1, 2020 | Jan 1, 2050 |
| Latvia | Jan 1, 2020 | Jan 1, 2050 |
| Malta | Jan 1, 2020 | Jan 1, 2050 |
| Netherlands | Jan 1, 2020 | Jan 1, 2050 |
| Norway | Jan 1, 2020 | Jan 1, 2050 |
| Poland | Jan 1, 2020 | Jan 1, 2050 |
| Portugal | Jan 1, 2020 | Jan 1, 2050 |
| Romania | Jan 1, 2020 | Jan 1, 2050 |
| Sweden | Jan 1, 2020 | Jan 1, 2050 |
| Slovenia | Jan 1, 2020 | Jan 1, 2050 |
| Slovakia | Jan 1, 2020 | Jan 1, 2050 |
| Türkiye | Jan 1, 2020 | Jan 1, 2050 |
| XI | Jan 1, 2020 | Jan 1, 2050 |
CN-MF-000006019No 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.69207567KXXWTXQ00018WOn the marketHollow Fiber Hemodialyzer high-flux69207567KXXWTXQ00018WOn the marketA.V. fistula needle sets for single use Revolving wing 1.2mm(18G)Red water stop clip69207567DJMCCZ0001W8On the marketA.V. fistula needle sets for single use Revolving wing 1.6mm(16G) Blue water stop clip69207567DJMCCZ0001W8On the marketHollow fiber hemodialyzer low-flux69207567KXXWTXQ00028YOn the market