- Role
- Country
- Date of registration
- Address
CN-MF-000014070Single Patient Use Powered Endo Cutter is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Golden Stapler Surgical Co., Ltd.. Placed on the EU market in Greece. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Dec 12, 2025
694691220049J9Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)06946912209114
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
1 warning 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 EL; available across 8 countries total.
| Country | On market since | Until |
|---|---|---|
| ELPrimary placement | Jul 30, 2025 | Jul 29, 2030 |
| Austria | Jul 30, 2025 | Jul 29, 2030 |
| Cyprus | Jul 30, 2025 | Jul 29, 2030 |
| Germany | Jul 30, 2025 | Jul 29, 2030 |
| France | Jul 30, 2025 | Jul 29, 2030 |
| Italy | Jul 30, 2025 | Jul 29, 2030 |
| Latvia | Jul 30, 2025 | Jul 29, 2030 |
| Portugal | Jul 30, 2025 | Jul 29, 2030 |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
06946912209114Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
694691220049J9Certificate No. G15 004954 0006 Rev. 00UDI 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.
1 packaging level registered — each level carries its own UDI-DI.
06946912209114× 1 unitBase unit86946912209110× 6 unitsEuropean Medical Device Nomenclature — the EU product classification assigned to this device.
H020301040299SINGLE PATIENT STRAIGHT LINEAR STAPLERS WITHOUT BLADE FOR VIDEOSURGERY – OTHERH020301040202SINGLE PATIENT STRAIGHT LINEAR STAPLERS WITHOUT BLADE FOR LAPAROSCOPYH020301040201SINGLE PATIENT STRAIGHT LINEAR STAPLERS WITHOUT BLADE FOR THORACOSCOPYNo certificate specifically references this device's Basic UDI-DI.
No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.