- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Feb 11, 2026
B-04250203220972Set für postoperative Autotransfusion 40 µm Filter - 1 Anschluss geschlossen, Blutsammelbeutel 1000ml und Drain und Trokar Ch.18/ 800/150 is an MDD-legacy 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.
DE-MF-0000049670521DE410200424No 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.(01)04250203220972
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 |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
04250203220972Basic 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-0425020322097221786UDI 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.
B0402INTRA- AND POSTOPERATIVE BLOOD COLLECTION AND REINFUSION ONLY DEVICES AND KITSPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →42502032PRI0134HOn the marketSchwerkraftdrainage 400 ml42502032PRI0154MOn the marketSet für postoperative Autotransfusion 1-fach mit Ersatzbeutel und Drain mit Trokar (Ch.14)B-04250203257190On the marketSet für postoperative Autotransfusion mit Ersatzbeutel und Drain mit Trokar (Ch.14)B-04250203218238On the marketSet für postoperative Autotransfusion, mit Ersatzbeutel und Drain mit Trokar (Ch.16)B-04250203210201On the marketSilikon-Thoraxkatheter gerade Ch.20, 6 Augen, Länge 520 mm mit 1 Kontraststreifen blau, Shore 70, bedruckt, getempert angefast, mit Wellenschnitt, steril42502032PRI04956On the marketNo certificate specifically references this device's Basic UDI-DI.