1428

Organization name

Sakura Finetek Europe B.V.

SRN

NL-MF-000023138

Manufacturer status

Active

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

• CW073

  EUDAMED did not publish a description for this code.
• CW081

  EUDAMED did not publish a description for this code.
• CW119

  EUDAMED did not publish a description for this code.
• CW158

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

  EUDAMED did not publish a description for this code.
• CW193

  EUDAMED did not publish a description for this code.
• CW194

  EUDAMED did not publish a description for this code.
• CW430

  EUDAMED did not publish a description for this code.
• CW444

  EUDAMED did not publish a description for this code.
• CW397

  EUDAMED did not publish a description for this code.
• CW416

  EUDAMED did not publish a description for this code.
• CW175

  EUDAMED did not publish a description for this code.
• CW225

  EUDAMED did not publish a description for this code.
• CW010

  EUDAMED did not publish a description for this code.

Primary placement in Netherlands; available across 32 countries total.

Trade name

not provided

UDI-DI code

08720177655484

Basic UDI-DI

8720177600057785FL

Reference / catalog number

1428

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

6 x 1L

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.

• W01030799HISTOLOGY / CYTOLOGY REAGENTS - OTHER