- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Jul 11, 2026
89042552MES_MEC30TVMirus™ Endocutter 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 Greece. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
18904255233505ME/BRC/STA/004(01)18904255233505
European Medical Device Nomenclature — the EU product classification assigned to this device.
H020301050102SINGLE PATIENT ARTICULATED LINEAR STAPLERS WITH BLADE FOR LAPAROSCOPY1 warning recorded — scroll inside the panel to see all entries.
"• Minimally invasive procedures should be performed only by persons having adequate training and familiarity with minimally invasive techniques. Consult medical literature relative to techniques, complications, and hazards prior to performance of any minimally invasive procedure. • Minimally invasive instruments may vary in diameter from manufacturer to manufacturer. When minimally invasive instruments and accessories from different manufacturers are employed together in a procedure, verify compatibility prior to initiation of the procedure. • Failure to properly follow the instructions may lead to serious surgical consequences, such as leakage or disruption. • When dividing major vascular structures, be sure to adhere to the basic surgical principle of proximal and distal control. • Before using, remove the staple retaining cap and observe the surface of the reload. The reload must be replaced with another reload if any colored drivers are visible. • Make sure tissue to be stapled is properly positioned in the jaws before stapling. Bunching or stretching of tissue could result in leakage, lack of hemostasis or disruption of staple line. • If the firing trigger is difficult to lock, reposition the instrument and take a smaller amount of tissue. • Prior to articulating and positioning the instrument jaws on tissue, make sure the jaws are in the open position. "
Primary placement in EL; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| ELPrimary placement | Oct 31, 2020 | 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.
1000316802RestrictedG70 105557 0008IssuedG15 105557 0007Issued1000214950IssuedNotified 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 →No certificate specifically references this device's Basic UDI-DI.