08-0001/FE

Organization name

R. Langenbrinck GmbH

SRN

DE-MF-000025266

Manufacturer status

Active

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

• CW083

  EUDAMED did not publish a description for this code.
• CW093

  EUDAMED did not publish a description for this code.
• CW094

  EUDAMED did not publish a description for this code.
• CW159

  EUDAMED did not publish a description for this code.
• CW167

  EUDAMED did not publish a description for this code.
• CW313

  EUDAMED did not publish a description for this code.
• CW306

  EUDAMED did not publish a description for this code.
• CW148

  EUDAMED did not publish a description for this code.

Primary placement in Germany; available across 1 country total.

Trade name

not provided

UDI-DI code

04262354732228

Basic UDI-DI

426235473PPS9

Reference / catalog number

08-0001/FE

Issuing entity

GS1

Risk category

IVDR Class A

Applicable legislation

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]

Status

On the market

Quantity

1

Additional product description

Shipping container, capacity 40 ml, 85 x 30 mm, half-filled with 4% formaldehyde, labeled with laboratory label and IVD marking

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

• W05020103SAMPLES TRANSPORT, BOTTLES

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