MEK-620I

Organization name

NIHON KOHDEN FIRENZE S.r.l.

SRN

IT-MF-000007607

Manufacturer status

Active

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

• CW041

  EUDAMED did not publish a description for this code.
• CW073

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

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

  EUDAMED did not publish a description for this code.
• CW106

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

  EUDAMED did not publish a description for this code.
• CW162

  EUDAMED did not publish a description for this code.
• CW166

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

  EUDAMED did not publish a description for this code.
• CW304

  EUDAMED did not publish a description for this code.

Primary placement in Italy; available across 1 country total.

Placed on the market in Italy; per-country availability dates not published.

Trade name

not provided

UDI-DI code

08054615270107

Basic UDI-DI

805461527IVD0001AY

Reference / catalog number

MEK-620I

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

—

Additional information URL

https://nkf.it/wp-content/uploads/IFU_A.pdf

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.

• W0103010105CBC-REAGENTS (CLEANING-/DILUTING-/LYSING-/SHEAT-FLUIDS)