- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on May 22, 2026
69257761000801Y4easyEndo™ E-Lite Single Use Powered Endoscopic Stapler is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Ezisurg Medical Co., Ltd.. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
CN-MF-000006742(01)06925776106005
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
6 warnings recorded — scroll inside the panel to see all entries.
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.
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 France; available across 5 countries total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Aug 7, 2025 | Oct 29, 2028 |
| Germany | Aug 6, 2025 | Oct 29, 2028 |
| Spain | Aug 6, 2025 | Oct 29, 2028 |
| Italy | Aug 6, 2025 | Oct 29, 2028 |
| Poland | Aug 20, 2025 | Oct 29, 2028 |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
06925776106005Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
69257761000801Y4P2UM60GUDI 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.
2 packaging levels registered — each level carries its own UDI-DI.
06925776106005× 1 unitBase unit16925776106002× 1 unit76925776106004× 3 unitsEuropean Medical Device Nomenclature — the EU product classification assigned to this device.
H020301050102SINGLE PATIENT ARTICULATED LINEAR STAPLERS WITH BLADE FOR LAPAROSCOPYH020301050101SINGLE PATIENT ARTICULATED LINEAR STAPLERS WITH BLADE FOR THORACOSCOPYH020201020201SINGLE PATIENT ARTICULATED LINEAR STAPLERS WITH BLADE FOR OPEN SURGERYPrimary 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.
HZ 2005388-1SupplementedNotified 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 →69257761000801Y4On the marketeasyEndo™ E-Lite Single Use Powered Endoscopic Stapler69257761000801Y4On the marketeasyEndo™ E-Lite Single Use Powered Endoscopic Stapler69257761000801Y4On the marketeasyEndo™ Lite Linear Cutting Stapler for Single Use69257761000311XEOn the marketeasyEndo™ Lite Linear Cutting Stapler for Single Use69257761000311XEOn the marketeasyEndo™ Lite Linear Cutting Stapler for Single Use69257761000311XEOn the marketNo certificate specifically references this device's Basic UDI-DI.