1R2256L

Organization name

Reagena Oy

SRN

FI-MF-000002804

Manufacturer status

Active

11 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.
• CW137

  EUDAMED did not publish a description for this code.
• CW138

  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.
• CW422

  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.
• CW010

  EUDAMED did not publish a description for this code.

Primary placement in Finland; available across 32 countries total.

Trade name

not provided

UDI-DI code

06430074450953

Basic UDI-DI

643007445102256SC76

Reference / catalog number

1R2256L

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

18

Additional product description

—

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

• W01030705FIXING REAGENTS (HISTOLOGY/CYTOLOGY)

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

Certificate health across this manufacturer's portfolio.