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EUDAMED last updated this device on Jun 19, 2026
4987670A0601RRMRT-2020 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Canon Inc.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
JP-MF-000013254(01)04987670101632
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.
CW999Sterile
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 14 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Jul 28, 2014 | Still on market |
| Austria | Sep 28, 2016 | Still on market |
| Bulgaria | Mar 26, 2024 | Still on market |
| Estonia | Sep 25, 2020 | Still on market |
| EL | Dec 8, 2023 | Still on market |
| Spain | Mar 11, 2015 | Still on market |
| Finland | Nov 17, 2014 | Still on market |
| France | Dec 19, 2018 | Still on market |
| Croatia | Sep 28, 2023 | Still on market |
| Italy | Dec 4, 2014 | Still on market |
| Netherlands | Nov 23, 2018 | Still on market |
| Poland | Sep 23, 2014 | Still on market |
| Portugal | Apr 1, 2017 | Still on market |
| Romania | Jul 6, 2021 | 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.
04987670101632Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
4987670A0601RRMRT-2020UDI 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.
Z11050104CLOSED MAGNET MRI SCANNERS WITH MAGNETIC FIELD LESS THAN OR EQUAL TO 2TPrimary 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.
4549292es01D8On the marketOptical Coherence Tomography OCT-A14549292oc01CWOn the marketMRT-1550 (Vantage Orian)4987670A0601RROn the marketINFX-8000V4987670A0101QYOn the marketINFX-8000F4987670A0101QYOn the marketMRT-15504987670A0601RROn 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.