Lamination Component Passive

Organization name

Integrum AB

SRN

SE-MF-000026900

Manufacturer status

Active

3 warnings recorded — scroll inside the panel to see all entries.

• Caution

  Symbol on label, described with text in IFU.

• Consult instructions for use

  Symbol on label, described with text in IFU.

• Do not use if package is damaged

  Symbol on label, described with text in IFU.

Primary placement in Sweden; available across 11 countries total.

Trade name

Lamination Component Passive

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.

07340152102409

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.

73401521accessoriesopra73

Reference / catalog number

2719

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

—

Additional information URL

No additional information URL provided by the manufacturer.

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.

• Y0699EXTERNAL PROSTHESES AND ORTHOSES - OTHER

• Class I medical devices in EUDAMED

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