- Organization name
- UDI-DI code
- Reference / catalog number
IT-MF-000027843MFLI0520-M000028349 is an EU MDR-regulated medical device on the European market. It is classified as Class I. Manufactured by B&T Spa. Placed on the EU market in Italy. Explore certificates, regulatory status and the official record on MD Atlas.
EUDAMED data as of Jun 25, 2026
EUDAMED last updated this device on May 28, 2026
802310300MATTD01Z5Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)08023103093399
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 | Jan 1, 2025 | 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.
08023103093399Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
802310300MATTD01Z5MFLI0520-M000028349UDI 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.
V080702NON ACTIVE ANTI-DECUBITUS MEDICAL MATTRESSESNo 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.No certificate specifically references this device's Basic UDI-DI.
802310300MATTD01Z5On the marketMSUR0215-M000000638802310300MATTD01Z5On the marketRAVA0120-R000002425802310300RETTD035MOn the marketRN380520-R000003169802310300RETTD035MOn the marketMREAXXX0425-M000051670802310300MATTD01Z5On the marketMTOPXXM0725-M000043965802310300MATTD01Z5On the market