KITMed 2.1

Organization name

AIT Austrian Institute of Technology GmbH

SRN

AT-MF-000002398

Manufacturer status

Active

1 warning recorded — scroll inside the panel to see all entries.

• CW011

  Patients with indication for intensive medicinal treatment are excluded from the use of KITMed. KITMed is not intended for use in emergency medical care. The patient must be informed that in the event of an emergency the family doctor or the local rescue or emergency medical service must be contacted directly. KITMed is not intended for the use in intensive care or for monitoring patients in intensive care. Patients with an indication for intensive care are excluded from the use of KITMed.

Primary placement in Austria; available across 2 countries total.

Trade name

not provided

UDI-DI code

09120109830139

Basic UDI-DI

912010983KITMed2NV

Reference / catalog number

KITMed 2.1

Issuing entity

GS1

Risk category

Class IIa

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

—

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

• V92MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES

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