KC2412

Organization name

Immundiagnostik AG

SRN

DE-MF-000020905

Manufacturer status

Active

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

• CW057

  EUDAMED did not publish a description for this code.
• CW085

  EUDAMED did not publish a description for this code.
• CW077

  EUDAMED did not publish a description for this code.
• CW075

  EUDAMED did not publish a description for this code.
• CW079

  EUDAMED did not publish a description for this code.
• CW082

  EUDAMED did not publish a description for this code.
• CW087

  EUDAMED did not publish a description for this code.
• CW091

  EUDAMED did not publish a description for this code.
• CW097

  EUDAMED did not publish a description for this code.
• CW099

  EUDAMED did not publish a description for this code.
• CW102

  EUDAMED did not publish a description for this code.
• CW105

  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

04050598011250

Basic UDI-DI

B-04050598011250

Reference / catalog number

KC2412

Issuing entity

GS1

Risk category

IVDD — General

Applicable legislation

IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]

Status

On the market

Quantity

1

Additional product description

The Immundiagnostik AG assay is intended for the quantitative determination of vitamin K1 and K2 in plasma and serum. For in vitro diagnostic use only.

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.

• W01019099CLINICAL CHEMISTRY REAGENTS - OTHER