- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 21, 2025
4963931YDM00002WGJP-MF-000011653(01)04963931146581
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 Spain; available across 12 countries total.
| Country | On market since | Until |
|---|---|---|
| SpainPrimary placement | Sep 21, 2021 | Still on market |
| Austria | Sep 21, 2021 | Still on market |
| Bulgaria | Sep 21, 2021 | Still on market |
| Germany | Sep 21, 2021 | Still on market |
| France | Sep 21, 2021 | Still on market |
| Hungary | Sep 21, 2021 | Still on market |
| Italy | Sep 21, 2021 | Still on market |
| Netherlands | Sep 21, 2021 | Still on market |
| Poland | Sep 21, 2021 | Still on market |
| Romania | Sep 21, 2021 | Still on market |
| Sweden | Sep 21, 2021 | Still on market |
| Türkiye | Sep 21, 2021 | Still on market |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
04963931146581Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
4963931YDM00002WG14658UDI 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.
L150201DENTAL RETRACTORS, REUSABLECheek Retractor Stemberg S is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by YDM CORPORATION. Placed on the EU market in Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
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 →No certificate specifically references this device's Basic UDI-DI.
4963931YDM00002WGOn the marketCheek Retractor Pigeon SS4963931YDM00002WGOn the marketCheek Retractor Stemberg L4963931YDM00002WGOn the marketColor Tray Premium for Lower Blue4963931YDM00005WNOn the marketColor Tray Premium for Lower Gold4963931YDM00005WNOn the marketColor Tray Premium for Lower Pink4963931YDM00005WNOn the marketNo 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.