- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Apr 9, 2026
805572802VDC0I0AXCONNECTION SCREW FOR SCREWED IN PROSTHESIS FOR OS TRANSFER COPING is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Edierre Implant System Srl. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
IT-MF-000027663No 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.(01)08055728020108
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 Italy; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Apr 6, 2005 | 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.
08055728020108Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
805572802VDC0I0AXP910000UDI 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.
Q010280PROSTHETIC DENTISTRY DEVICES - ACCESSORIESPrimary 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.
B-08055728022140On the marketCONNECTION SCREW FOR CLOSED SPOON TRANSFER COPING D. 3.3805572802VDC0I0AXOn the marketCONNECTION SCREW FOR CLOSED SPOON TRANSFER COPING D. 3.75/4.2/4.5/5.0805572802VDC0I0AXOn the marketCS TRANSFER COPING X ANGLED AND MONOBLOCCO ABUTMENT FOR SCREWED-IN PROSTHESIS D. 3.3/3.75/4.2/4.5 Cone A805572802TRA000C9On the marketDIGITAL SCANBODY FOR PROSTHETICS PROTHESIS805572802SCNPA0FVOn the marketDIGITAL SCANBODY FOR PROSTHETICS PROTHESIS - CONE B - D. 3.3805572802SCNPA0FVOn the market