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EUDAMED last updated this device on Mar 16, 2026
805573143VCA00000ASTR.SFEVITE ASTRAGALICA FORATA Ø8MM L30MM 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)08055731432707
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.
08055731432707Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
805573143VCA00000ASTR.SFE5000401FSTUDI 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.
P09120699BONE FIXATION SCREWS, TENDON AND LIGAMENT SYNTHESIS SCREWS - 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 →805573143BSS000HEADLESSGNOn the marketVITE A COMPRESSIONE HEADLESS Ø8.0MM L170MM FILETTO COMPLETO ST805573143BSS000HEADLESSGNOn the marketVITE A COMPRESSIONE HEADLESS Ø8.0MM L170MM FILETTO CORTO F33MM ST805573143BSS000HEADLESSGNOn the marketVITE ASTRAGALICA Ø6.5MM L25MM TI ST805573143VCA0TIT.ASTR.SLAOn the marketVITE ASTRAGALICA Ø6.5MM L30MM TI ST805573143VCA0TIT.ASTR.SLAOn the marketVITE ASTRAGALICA Ø6.5MM L35MM TI ST805573143VCA0TIT.ASTR.SLAOn the marketNo certificate specifically references this device's Basic UDI-DI.
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.
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