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EUDAMED last updated this device on Jul 17, 2026
890607090MES_MLS31Z6Mirus™ Linear Stapler 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.
18906070909900ME/BRC/034(01)18906070909900
European Medical Device Nomenclature — the EU product classification assigned to this device.
H020201010102SINGLE PATIENT STRAIGHT LINEAR STAPLERS WITHOUT BLADE FOR OPEN SURGERY1 warning recorded — scroll inside the panel to see all entries.
"• This instrument is intended for use by medical professional only. • Do not use MirusTM Linear stapler and MirusTM Linear Stapler Reload on conditions other than intended use. • Use MirusTM Linear stapler Reload together with MirusTM Linear stapler only. • Preoperative radiotherapy may result in tissue changes that may cause the tissue thickness to exceed the indicated range for the selected staple size. Careful consideration should be given to any pre-surgical treatment that the patient may have undergone and in corresponding selection of staple size. Selection of staple size may vary depending on patients's pre-surgical treatment. • Each component in the package must be used in the manner indicated. • 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. • Always inspect the staple line for hemostasis, Metal clips, staples, or sutures contained in the area to be stapled may affect the integrity of the staple line. Corrective action, if required, may include the use of sutures or electrocautery. • Verify the compatibility of Reload, instruments and accessories prior to using the instrument. • MirusTM linear Staplers are provided STERILE and are intended for multiple use during a single surgical procedure for one patient. DISCARD AS MEDICAL WASTE AFTER USE. DO NOT RESTERILIZE. • The MirusTM Linear Stapler Reload is provided STERILE and is intended for use in a SINGLE procedure only. DISCARD AS MEDICAL WASTE AFTER USE. DO NOT RESTERILIZE.• Each MirusTM Linear Stapler Reload will fit and operate properly in only the staplers designed for use with the Reload. Attempting to use a Reload in any instrument other than for which it has been designed will result in stapler malfunction. "
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.
1000316802Restricted1000214950IssuedNotified 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 →890607090MES_MLC32WQOn the marketMirus™ Linear Stapler890607090MES_MLS31Z6On the marketMirus™ Linear Stapler890607090MES_MLS31Z6On the marketMirus™ Linear Stapler890607090MES_MLS31Z6On the marketMonik™ Disposable Endoscopic Trocar89042552MES_DET36TTOn the marketMonik™ Disposable Endoscopic Trocar89042552MES_DET36TTOn the marketNo certificate specifically references this device's Basic UDI-DI.