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EUDAMED last updated this device on Sep 1, 2026
B-00860005202805MTx.100 is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by Marker Americas LP. Placed on the EU market in Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
00860005202805MTx.100(01)00860005202805
European Medical Device Nomenclature — the EU product classification assigned to this device.
B030299APHERESIS THERAPY DEVICES - OTHER25 warnings recorded — scroll inside the panel to see all entries.
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Carefully read these Instructions for Use before performing treatment with the MTx.100 Plasma Adsorption Column. Also consult and understand the plasma separation device Instructions for Use.
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Primary placement in Spain; available across 5 countries total.
| Country | On market since | Until |
|---|---|---|
| SpainPrimary placement | Feb 21, 2020 | Still on market |
| Germany | Feb 21, 2020 | Still on market |
| France | Feb 21, 2020 | Still on market |
| Italy | Feb 21, 2020 | Still on market |
| Portugal | Feb 21, 2020 | Still on market |
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The MTx.100 Plasma Adsorption Column is for single use only. DO NOT REUSE due to risk of infection or contamination.
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The MTx.100 Plasma Adsorption Column is not to be used after the expiration date has passed.
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Do not re-sterilize.
Examine each MTx.100 Plasma Adsorption Column tray prior to use. Do not use a MTx.100 that appears to have been damaged or whose sterile barrier seal has been broken.
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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.
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 →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 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.No certificate specifically references this device's Basic UDI-DI.
This device is not currently linked to any other device.