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US-MF-000000765G70 104609 0008INTERCEPT Processing Set for Plasma is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class III. Manufactured by Cerus Corporation. Placed on the EU market in Austria. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Mar 7, 2025
872058919008PLS2RPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)18717953197105
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
1 warning recorded — scroll inside the panel to see all entries.
Refer to Instructions for Use
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 Austria; available across 31 countries total.
| Country | On market since | Until |
|---|---|---|
| AustriaPrimary placement | Oct 20, 2006 | Still on market |
| Belgium | Oct 20, 2006 | Still on market |
| Bulgaria | Oct 20, 2006 | Still on market |
| Cyprus | Oct 20, 2006 | Still on market |
| Czechia | Oct 20, 2006 | Still on market |
| Germany | Oct 20, 2006 | Still on market |
| Denmark | Oct 20, 2006 | Still on market |
| Estonia | Oct 20, 2006 | Still on market |
| EL | Oct 20, 2006 | Still on market |
| Spain | Oct 20, 2006 | Still on market |
| Finland | Oct 20, 2006 | Still on market |
| France | Oct 20, 2006 | Still on market |
| Croatia | Oct 20, 2006 | Still on market |
| Hungary | Oct 20, 2006 | Still on market |
| Ireland | Oct 20, 2006 | Still on market |
| Iceland | Oct 20, 2006 | Still on market |
| Italy | Oct 20, 2006 | Still on market |
| Liechtenstein | Oct 20, 2006 | Still on market |
| Lithuania | Oct 20, 2006 | Still on market |
| Luxembourg | Oct 20, 2006 | Still on market |
| Latvia | Oct 20, 2006 | Still on market |
| Malta | Oct 20, 2006 | Still on market |
| Netherlands | Oct 20, 2006 | Still on market |
| Norway | Oct 20, 2006 | Still on market |
| Poland | Oct 20, 2006 | Still on market |
| Portugal | Oct 20, 2006 | Still on market |
| Romania | Oct 20, 2006 | Still on market |
| Sweden | Oct 20, 2006 | Still on market |
| Slovenia | Oct 20, 2006 | Still on market |
| Slovakia | Oct 20, 2006 | Still on market |
| Türkiye | Oct 20, 2006 | 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.
18717953197105Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
872058919008PLS2RINT3103UDI 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.
B010199BLOOD COLLECTION BAGS AND KITS - OTHERCertificate health across this manufacturer's portfolio.
G70 104609 0007AmendedG10 104609 0014IssuedG12 104609 0009IssuedG12 104609 0010IssuedG70 104609 0008IssuedNotified 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 →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 →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 →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 →