71240

Organization name

Kemetyl AB

SRN

SE-MF-000045073

Manufacturer status

Active

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

• CW043

  EUDAMED did not publish a description for this code.
• CW058

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

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

  EUDAMED did not publish a description for this code.
• CW139

  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.
• CW314

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

  EUDAMED did not publish a description for this code.
• CW148

  EUDAMED did not publish a description for this code.
• CW038

  EUDAMED did not publish a description for this code.

Primary placement in Sweden; available across 1 country total.

Trade name

not provided

UDI-DI code

07311850712405

Basic UDI-DI

731185GMN600Y8

Reference / catalog number

71240

Issuing entity

GS1

Risk category

Class I

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

1

Additional product description

—

Additional information URL

https://www.kemetyl.se/

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.

• D0799ALCOHOLS FOR THE DISINFECTION OF MEDICAL DEVICES - OTHER