- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Jul 20, 2026
803413929BELPUMPDRAIN1aJTDRENTECH CLOSED SERBATOIO 400 ML C/SACCA is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Redax S.p.A.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
08034139293981226011 packaging level registered — each level carries its own UDI-DI.
08034139293981× 1 unitBase unit18034139293988× 10 units(01)08034139293981
European Medical Device Nomenclature — the EU product classification assigned to this device.
A0601010102DRAINAGE SYSTEMS WITH RESERVOIR6 warnings recorded — scroll inside the panel to see all entries.
IT-MF-000019320The 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 Italy; available across 5 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Jan 1, 2001 | Still on market |
| Germany | Jan 1, 2001 | Still on market |
| Spain | Jan 1, 2001 | Still on market |
| France | Jan 1, 2001 | Still on market |
| Poland | Jan 1, 2001 | 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.
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.
803413929BELPUMPDRAIN1aJTOn the marketDRENTECH CLOSED 400 ML CIRCUITO CHIUSO, DRENAGGIO SPIRALATO CON AGO CH 19803413929BELPUMPDRAIN1aJTOn the marketDRENTECH CLOSED SERBATOIO 100 ML C/SACCA803413929BELPUMPDRAIN1aJTOn the marketDRENTECH CLOSED SERBATOIO 400 ML C/SACCA803413929BELPUMPDRAIN1aJTOn the marketDRENTECH CLOSED SERBATOIO 400 ML C/SACCA CIRCUITO CHIUSO803413929BELPUMPDRAIN1aJTOn the marketDRENTECH CLOSED SET 400 ML CIRCUITO CHIUSO E DRENAGGIO SPIRALATO CON AGO CH 10803413929BELPUMPDRAIN1aJTOn 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.