- Role
- Country
- Date of registration
- Address
ES-MF-000009479No 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.Rotatory impression coping 30º Tappered abutment Std Osseous Inh.Std/Max with screw is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by MOZO GRAU SA. Placed on the EU market in Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Jun 1, 2026
84354826IMPRESSIONSQPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)08435482602244
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 3 countries total.
| Country | On market since | Until |
|---|---|---|
| SpainPrimary placement | — | Still on market |
| Poland | — | Still on market |
| Romania | — | 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.
08435482602244Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
84354826IMPRESSIONSQ13205530UDI 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 DENTISTRYNo certificate specifically references this device's Basic UDI-DI.
84354826CASTABLE4LOn the marketRotatory castable post for 10º Tappered abutment Osseous/Inhex with screw84354826CASTABLE4LOn the marketRotatory impression coping for 10º Tappered abutment Osseous/Inhex84354826IMPRESSIONSQOn the marketRotatory impression coping for 10º Tappered abutment Max Osseous/Inhex84354826IMPRESSIONSQOn the marketRotatory impression coping for 10º Tappered abutment Osseous/Inhex Maxiwith screw84354826IMPRESSIONSQOn the marketRotatory impression coping for 10º Tappered abutment Osseous/Inhex with screw84354826IMPRESSIONSQOn the market