Organization name

B BRAUN MEDICAL, S.A.

SRN

ES-MF-000015264

Manufacturer status

Active

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

• Single patient multiple use
• Consult instructions for use
• Do not use past indicated date

Primary placement in Spain; available across 27 countries total.

Trade name

Linovera®

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.

04046955623976

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.

40392390000016522P

Reference / catalog number

492972

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 IIa

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

LINOVERA 30 ML EN/MS

Additional information URL

https://eifu.bbraun.com/

Clinical sizes

• 30 ML

1 packaging level registered — each level carries its own UDI-DI.

• 04046955623976× 1 unitBase unit
  • 04046955639878× 20 units

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

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

• M04041501DRESSINGS IN SOLUTIONS, EMULSIONS, GELS, POWDERS WITH HERBAL COMPONENTS

• Class IIa medical devices in EUDAMED

Certificate health across this manufacturer's portfolio.

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