- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 20, 2026
8055731430ERKITCUSTOM.SXSCLICKIT SHOULDER BARRE CORTE SENZA STRUMENTARIO ST is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by Mikai s.p.a.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
IT-MF-000030732(01)08055400672410
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
4 warnings recorded — scroll inside the panel to see all entries.
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 9 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | — | Still on market |
| Germany | — | Still on market |
| EL | — | Still on market |
| Spain | — | Still on market |
| Croatia | — | Still on market |
| Ireland | — | Still on market |
| Poland | — | Still on market |
| Portugal | — | Still on market |
| Slovakia | — | 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.
08055400672410Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
8055731430ERKITCUSTOM.SXS5000630STA1UDI 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.
P09120499EXTERNAL BONE FIXATION SYSTEMS - OTHERPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Certificate health across this manufacturer's portfolio.
ITH 1343576 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 →No certificate specifically references this device's Basic UDI-DI.
8055731430ERKITCUSTOM.SXSOn the marketCLICKIT PELVIS ST8055731430ERKITCUSTOM.SXSOn the marketCLICKIT SHOULDER A UNA BARRA ST8055731430ERKITCUSTOM.SXSOn the marketCLICKIT SHOULDER SENZA STRUMENTARIO ST8055731430ERKITCUSTOM.SXSOn the marketCLIP PER FILI Ø1.8MM ST8055731430ER0000CLAMP.SRTOn the marketCLIP PER FILI Ø1.8MM TI ST8055731430ER00TICLAMP.SZBOn the market