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JP-MF-000011653Ortho.Pliers EVER C. 419 Nance Closing Loop 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.
EUDAMED last updated this device on May 15, 2025
4963931YDM00001WEPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)04963931274192
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.
04963931274192Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
4963931YDM00001WE27419UDI 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.
L150702ORTHODONTIC PLIERS, REUSABLENo certificate specifically references this device's Basic UDI-DI.
4963931YDM00005WNOn the marketOrtho.Pliers EVER C. 413 Bracket Removing T/C4963931YDM00001WEOn the marketOrtho.Pliers EVER C. 416 Tweed Loop Forming4963931YDM00001WEOn the marketOrtho.Pliers EVER C.426 Lingual Hollow Chop4963931YDM00001WEOn the marketOrtho.Pliers EVER Classic 410 Band Contouring4963931YDM00001WEOn the marketOrtho.Pliers EVER Classic 411 Band Margin4963931YDM00001WEOn 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.