08-0050/FX

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

04262354732372

Basic UDI-DI

426235473Scinti4R

Reference / catalog number

08-0050/FX

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

Scintillation Tube volume 20 ml half filled with 4% formaldehyde labeled with dangerlabel and IVD marking, with white srew cap

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