EUDAMED last updated this device on Aug 10, 2026

Mirus™ Endocutter

89042552MES_MEC30TV

On the marketClass IIa

Applicable legislation: —
Organization name: Meril Endo Surgery Pvt. Ltd.
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 →: 18904255233499
Reference / catalog number: ME/BRC/STA/004

Regulatory classification unavailableThis product's Basic UDI record hasn't been published in EUDAMED yet. Classification and compliance details will appear automatically once EUDAMED publishes it.

Mirus™ Endocutter is an EU-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.

Device identification

Trade name: Mirus™ Endocutter
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 →: 18904255233499
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 →: 89042552MES_MEC30TV
Reference / catalog number: ME/BRC/STA/004
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 →: GS1

Classification

Risk category: Class IIa
Applicable legislation: —
Status: On the market

Device details

Quantity: 1
Additional product description: Mirus™ Endocutter places two, double or triple-staggered reload which on firing simultaneously divide the tissue between the two rows. Mirus™ Endocutter is available in 3 different shaft lengths i.e. small, medium and large and furnished without a reload.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)18904255233499

UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

H020301050102SINGLE PATIENT ARTICULATED LINEAR STAPLERS WITH BLADE FOR LAPAROSCOPY

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

Consult instructions for use
"• 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. "

Compliance flags

Safety

Direct marking

Regulatory

Sterilization

Lifecycle

New device

Market distribution

Primary placement in EL; available across 1 country total.

Country	On market since	Until
ELPrimary placement	Oct 31, 2020	Still on market

Mirus™ Endocutter

Device identification

Classification

Device details

UDI-PI traceability

UDI-DI DataMatrix

UDI-PI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Regulatory

Lifecycle

Market distribution

Related searches

Device identification

Classification

Device details

Manufacturer information

UDI-PI traceability

UDI-DI DataMatrix

UDI-PI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Regulatory

Lifecycle

Certificates

Certificates covering this device

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Market distribution

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Manufacturer information

Certificates covering this device

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Certificates