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EUDAMED last updated this device on Apr 16, 2026
47198815613VN1313USS16250A1 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by MEM Dental Technology Co., Ltd. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
047198815661801313USS16250A1(01)04719881566180
European Medical Device Nomenclature — the EU product classification assigned to this device.
Q010404ORTHODONTIC ELASTICS, CHAINS AND SPRINGS2 warnings recorded — scroll inside the panel to see all entries.
Contraindicated in patients with known hypersensitivity to nickel or cobalt, conditions that increase aspiration risk, severe periodontal disease, uncontrolled parafunctional habits, or medical conditions that contraindicate orthodontic treatment. Not intended for patients aged 10 years or under. Refer to the Instructions for Use for full details.
The device is non-implantable and intended for temporary orthodontic use. Patients should inform MRI or radiology personnel of the presence of orthodontic devices prior to imaging to ensure patient safety and diagnostic accuracy.
Primary placement in France; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | — | Still on market |
TW-MF-000003514The 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.
View in glossary →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.
View in glossary →Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
View in glossary →CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
View in glossary →Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
View in glossary →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 →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →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.
View in glossary →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.
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.