06000

Trade name

not provided

UDI-DI code

08022386020238

Basic UDI-DI

8022386EDP01526063RB

Reference / catalog number

06000

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

Afterbite electrostimulator that, through the release of electrical micro-impulses, can relieve local symptoms - itching and inflammation - caused by mosquito bites

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

European Medical Device Nomenclature — the EU product classification assigned to this device.

• V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER

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

• CW011

  DO NOT USE on patients wearing a cardiac pacemaker, implanted defibrillator, or other implanted metallic or electronic device; on patients diagnosed with heart disease or epilepsy; on pregnant women; on children under 6 months. DO NOT USE on open wounds or rashes, or over infected or pathological or abnormal skin conditions, on bleeding or secreting areas and on mucous membranes; near flammable liquids or gas or if you have used an insect repellent and/or flammable substances (for example: perfume, deodorant, etc), as this device can ignite flammable substances; with wet hands or on wet skin.
• CW010

  Read the warnings
• CW018

  EUDAMED did not publish a description for this code.

No certificate specifically references this device's Basic UDI-DI.