- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Feb 6, 2026
42502032PRI04752Kapillardrain perforiert, Ø = 12 mm, L = 300 mm mit Röntgenkontraststreifen, steril is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Primed Halberstadt Medizintechnik GmbH. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
04250203207867214592 packaging levels registered — each level carries its own UDI-DI.
04250203207867× 1 unitBase unit04250203246446× 10 units04250203246453× 36 unitsDE-MF-000004967(01)04250203207867
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
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 1 country total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | — | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
A0601010403FLAT AND LAMELLAR DRAINAGESPrimary 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 →42502032PRI04752On the marketJ.P.-Flachdrain B = 7 mm L = 200 mm, vollperforiert42502032PRI04752On the marketKapillardrain perforiert, Ø = 10 mm, L = 300 mm mit Röntgenkontraststreifen, steril42502032PRI04752On the marketKapillardrain perforiert, Ø = 6 mm, L = 300 mm mit Röntgenkontraststreifen, steril42502032PRI04752On the marketKapillardrain perforiert, Ø = 8 mm, L = 300 mm mit Röntgenkontraststreifen, steril42502032PRI04752On the marketKapillardrain, B = 10 mm, L = 300 mm mit Röntgenkontraststreifen, steril42502032PRI04752On the marketNo certificate specifically references this device's Basic UDI-DI.
Certificate health across this manufacturer's portfolio.
0521GB448260910Reissued0521GB448260630SupplementedNotified 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 →