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EUDAMED last updated this device on Apr 29, 2026
805901874FTCAG6KF03 Cuscino in fibra cava siliconata con impuntura centrale 48x48 cm is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Capelli S.r.l.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
08059018743166KF034848(01)08059018743166
European Medical Device Nomenclature — the EU product classification assigned to this device.
V08030102NON-ACTIVE ANTI-DECUBITUS MEDICAL CUSHIONSIT-MF-000008232The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Primary placement in Italy; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | — | Still on market |
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 →No 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.805901874FTCAG6On the marketKF01 Siliconized hollow fiber cylinder cushion cm 46x46805901874FTCAG6On the marketKF01 Siliconized hollow fiber cylinder cushion cm 58x42805901874FTCAG6On the marketKF03 Siliconized hollow fiber cushion with central stitching cm 44x44805901874FTCAG6On the marketKF03 Siliconized hollow fiber cushion with central stitching cm 60x44805901874FTCAG6On the marketKF05 Wheelchair comfort kit805901874FTCAG6On the marketNo certificate specifically references this device's Basic UDI-DI.