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EUDAMED last updated this device on Jul 13, 2026
B-06974267893849Rooter Universal – Contra-angle is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Foshan COXO Medical Instrument Co., Ltd.. Placed on the EU market in Greece. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0697426789384908.970.00.011.FKCN-MF-000001682DD 60151346 0001(01)06974267893849
1 warning recorded — scroll inside the panel to see all entries.
Use with caution in patients with hemophilia or heart disease, pregnant women and children. Patients or operators with a pacemaker should use an electric-motor-driven handpiece with caution.
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 1 country total.
| Country | On market since | Until |
|---|---|---|
| ELPrimary placement | Mar 1, 2024 | Jul 13, 2026 |
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z12110101DENTAL TREATMENT UNITSPrimary 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.
Certificate health across this manufacturer's portfolio.
HZ 2182788-1IssuedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →