- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Jul 9, 2026
890607090MES_MLC32WQMirus™ Linear Cutter is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Meril Endo Surgery Pvt. Ltd.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
18906070909566ME/BRC/035(01)18906070909566
European Medical Device Nomenclature — the EU product classification assigned to this device.
H020201010101SINGLE PATIENT STRAIGHT LINEAR STAPLERS WITH BLADE FOR OPEN SURGERY1 warning recorded — scroll inside the panel to see all entries.
"•This instrument is intended for use by medical professional only. •Use MirusTM Linear Cutter Reload together with MirusTM Linear Cutter only. •Preoperative radiotherapy may result in changes to tissue. These changes may, for example, cause the tissue thickness to exceed the indicated range for the selected staple size. Careful consideration should be given to any pre-surgical treatment the patient may have undergone and in corresponding selection of staple size. •The linear cutters are provided sterile and are intended for multiple use during a single procedure. Discard after use. Do not resterilize. •The Reloads are provided sterile and are intended for use in a single procedure only. Discard after use. Do not resterilize. •Different types of Reloads are only compatible with corresponding linear cutters. Incompatible linear cutters and Reloads will result in unacceptable staple formation. •Ensure to select a Reload with the appropriate staple size for the tissue thickness. Overly thick or thin tissue may result in unacceptable staple formation. •Verify the compatibility of cartridge (Reload), instruments and accessories prior to using the instrument. •Visually inspect that there is no inclusion of unintended anatomic structures within the staple line. •Make sure that no metal clips or other obstructions are incorporated into the instrument jaw when positioning the stapler on the application site, otherwise the stapling may not form properly. •Tissue thickness should be carefully evaluated before firing any linear cutter. Refer to the specification chart and the warning & precautions. •The instrument should not be used on tissue such as liver or spleen where compressibility is such that closure of the instrument would be destructive. "
Primary placement in Italy; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Mar 18, 2016 | Still on market |
IN-MF-000010999The 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.
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 →Certificate health across this manufacturer's portfolio.
1000316802RestrictedNotified 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.
G70 105557 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.
G15 105557 0007IssuedNotified 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.
1000214950IssuedNotified 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.
890607090MES_MLC32WQOn the marketMirus™ Linear Cutter890607090MES_MLC32WQOn the marketMirus™ Linear Cutter890607090MES_MLC32WQOn the marketMirus™ Linear Cutter890607090MES_MLC32WQOn the marketMirus™ Linear Cutter890607090MES_MLC32WQOn the marketMirus™ Linear Cutter890607090MES_MLC32WQOn the marketNo certificate specifically references this device's Basic UDI-DI.