- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Aug 4, 2026
3660812A0400030HEKit de base is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by VYGON. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0366081216369980199.5421 packaging level registered — each level carries its own UDI-DI.
03660812163699× 1 unitBase unit53660812163694× 24 units(01)03660812163699
European Medical Device Nomenclature — the EU product classification assigned to this device.
A99DEVICES FOR ADMINISTRATION, WITHDRAWAL AND COLLECTION - OTHERFR-PR-000001873The 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.
View in glossary →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.
View in glossary →Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
View in glossary →CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
View in glossary →Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →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.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →3660812A0400015HJOn the marketIV-Versorungs-Set3660812A0400015HJOn the marketKatheter Set Cathéter3660812A0400045HTOn the marketKit de base Ath3660812A0400030HEOn the marketKit de insertie CVC CU halat de unica folosinta3660812A0400054HUOn the marketKit impianto CVC AV013660812A0400045HTOn the marketCertificate health across this manufacturer's portfolio.
39447SupplementedNotified 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.
No certificate specifically references this device's Basic UDI-DI.