Organization name

Levabo ApS

SRN

DK-MF-000014646

Manufacturer status

Active

Primary placement in Denmark; available across 21 countries total.

Trade name

Levaflex Twin - 90*200*14

UDI-DI code

Primary DI

The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.

05711014701566

Basic UDI-DI

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.

5711014LEVAFLEXT5

Reference / catalog number

70156

Issuing entity

UDI issuing entities

Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.

GS1

Risk category

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.

Class I

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

1

Additional product description

Levaflex support for prevention of pressure ulcer

Additional information URL

http://www.levabo.dk/

Clinical sizes

No clinical sizes registered for this device.

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

European Medical Device Nomenclature — the EU product classification assigned to this device.

• V080702NON ACTIVE ANTI-DECUBITUS MEDICAL MATTRESSES

• Class I medical devices in EUDAMED

No certificate specifically references this device's Basic UDI-DI.