- Role
- Country
- Date of registration
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IT-MF-000028795IMPRESSION COPING CLOSED TRAY CAP is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Zirkonzahn SRL. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on May 25, 2026
++D800IMPRCOP01CVPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
D800BSAQ00010
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.
2 warnings recorded — scroll inside the panel to see all entries.
OTHER
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 Italy; available across 32 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Jul 22, 2025 | Still on market |
| Austria | Jul 22, 2025 | Still on market |
| Belgium | Jul 22, 2025 | Still on market |
| Bulgaria | Jul 22, 2025 | Still on market |
| Cyprus | Jul 22, 2025 | Still on market |
| Czechia | Jul 22, 2025 | Still on market |
| Germany | Jul 22, 2025 | Still on market |
| Denmark | Jul 22, 2025 | Still on market |
| Estonia | Jul 22, 2025 | Still on market |
| EL | Jul 22, 2025 | Still on market |
| Spain | Jul 22, 2025 | Still on market |
| Finland | Jul 22, 2025 | Still on market |
| France | Jul 22, 2025 | Still on market |
| Croatia | Jul 22, 2025 | Still on market |
| Hungary | Jul 22, 2025 | Still on market |
| Ireland | Jul 22, 2025 | Still on market |
| Iceland | Jul 22, 2025 | Still on market |
| Liechtenstein | Jul 22, 2025 | Still on market |
| Lithuania | Jul 22, 2025 | Still on market |
| Luxembourg | Jul 22, 2025 | Still on market |
| Latvia | — | Still on market |
| Malta | Jul 22, 2025 | Still on market |
| Netherlands | Jul 22, 2025 | Still on market |
| Norway | Jul 22, 2025 | Still on market |
| Poland | Jul 22, 2025 | Still on market |
| Portugal | Jul 22, 2025 | Still on market |
| Romania | Jul 22, 2025 | Still on market |
| Sweden | Jul 22, 2025 | Still on market |
| Slovenia | Jul 22, 2025 | Still on market |
| Slovakia | Jul 22, 2025 | Still on market |
| Türkiye | — | Still on market |
| XI | Jul 22, 2025 | 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.
D800BSAQ00010Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
++D800IMPRCOP01CVBSAQ0001UDI 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.
Q010207DENTAL IMPRESSION DEVICES FOR PROSTHETIC DENTISTRY++D800ZR001001FEOn the marketICE TRANSLUCENT PLUS COLOURED++D800ZR001001FEOn the marketICE TRANSLUCENT PLUS DISPERSIVE++D800ZR001001FEOn the marketIMPRESSION COPING CONNECT++D800IMPRCOP01CVOn the marketIMPRESSION COPING OPEN TRAY HEX++D800IMPRCOP01CVOn the marketIMPRESSION COPING OPEN TRAY PIN++D800IMPRCOP01CVOn the marketCertificate health across this manufacturer's portfolio.
207/MDRSupplementedNotified 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 →No certificate specifically references this device's Basic UDI-DI.