- Role
- Country
- Date of registration
- Address
CN-MF-000030050Operation Microscope is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by 66 VISION TECH CO., LTD.. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Mar 29, 2026
6951090800SOMDEPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)06951090800022
The 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.
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 32 countries total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Feb 2, 2000 | Nov 27, 2099 |
| Austria | Feb 2, 2022 | Nov 27, 2099 |
| Belgium | Jul 3, 2020 | Dec 4, 2099 |
| Bulgaria | Jun 10, 2020 | Dec 5, 2099 |
| Cyprus | Feb 2, 2000 | Nov 27, 2099 |
| Czechia | Feb 2, 2000 | Nov 27, 2099 |
| Germany | Feb 2, 2000 | Nov 27, 2099 |
| Denmark | Feb 2, 2000 | Nov 27, 2099 |
| Estonia | Feb 2, 2000 | Nov 27, 2099 |
| EL | Jan 28, 2004 | Nov 27, 2099 |
| Spain | Feb 2, 2000 | Nov 27, 2099 |
| Finland | Feb 2, 2000 | Dec 4, 2099 |
| Croatia | Jan 29, 2020 | Nov 27, 2099 |
| Hungary | Feb 2, 2000 | Nov 27, 2099 |
| Ireland | Feb 2, 2000 | Nov 27, 2099 |
| Iceland | Feb 2, 2000 | Dec 4, 2099 |
| Italy | Feb 2, 2000 | Nov 27, 2099 |
| Liechtenstein | Feb 2, 2000 | Dec 4, 2099 |
| Lithuania | Feb 2, 2000 | Nov 27, 2099 |
| Luxembourg | Feb 2, 2000 | Nov 27, 2099 |
| Latvia | Feb 2, 2000 | Nov 27, 2099 |
| Malta | Feb 2, 2000 | Nov 20, 2099 |
| Netherlands | Feb 2, 2000 | Nov 27, 2099 |
| Norway | Feb 2, 2000 | Nov 27, 2099 |
| Poland | Feb 2, 2000 | Nov 27, 2099 |
| Portugal | Feb 2, 2000 | Nov 27, 2099 |
| Romania | Feb 2, 2000 | Nov 27, 2099 |
| Sweden | Feb 2, 2000 | Nov 20, 2099 |
| Slovenia | Feb 2, 2000 | Nov 27, 2099 |
| Slovakia | Feb 2, 2000 | Nov 20, 2099 |
| Türkiye | Feb 2, 2000 | Nov 27, 2099 |
| XI | Feb 2, 2000 | Nov 27, 2099 |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
06951090800022Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
6951090800SOMDEXI-AR-000001836UDI 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.
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z12011101OPERATIVE MICROSCOPESNo 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.