- Role
- Country
- Date of registration
- Address
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.CLOSED SPOON TRANSFER COPING FOR SCREWED IN PROSTHESIS STRAIGHT ABUTMENT D. 3.3 Cone B 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.
EUDAMED last updated this device on Apr 9, 2026
805572802TRA000C9Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)08055728020283
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.
08055728020283Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
805572802TRA000C9P933300UDI 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 - ACCESSORIESNo certificate specifically references this device's Basic UDI-DI.
B-08055728022539On the marketCAPS IN TI FOR STRAIGHT ABUTMENT FOR SCREWED IN PROSTHESIS with two secondary connection screwsB-08055728023420On the marketCAPS IN TI STRAIGHT ABUTMENT FOR SCREWED IN PROSTHESIS with two secondary connection screwsB-08055728023437On the marketCLOSED SPOON TRANSFER COPING FOR SCREWED IN PROSTHESIS STRAIGHT ABUTMENT D. 3.75/4.2/4.5 Cone B805572802TRA000C9On the marketCLOSED SPOON TRANSFER COPING with connection screw and cap D. 4.2 T3805572802TRA000C9On the marketCLOSED SPOON TRANSFER COPING with connection screw and cap D. 4.2 T5805572802TRA000C9On the market