ANIKA

Organization name

NOVAVISION GROUP

SRN

IT-MF-000024333

Manufacturer status

Active

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• CW010

  EUDAMED did not publish a description for this code.

Primary placement in Italy; available across 2 countries total.

Trade name

ANIKA

UDI-DI code

08059340930012

Basic UDI-DI

805934093N011848

Reference / catalog number

380800000335

Issuing entity

GS1

Risk category

Class IIb

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

The Anika equipment is a medical device that consists in the administration of CO2 subcutaneously and intradermally for therapeutic purposes through localised micro-injections using extremely thin needles (for example 30G), commonly used in mesotherapy. Delivery takes place in a controlled manner and the treatment involves replacing the needle for each patient to ensure the safety of the treatment. This practice is known as “carboxytherapy”, a therapy without toxicity risks: our body naturally produces carbon dioxide, therefore no risks are involved, it is therefore a non-toxic and non-hazardous system.

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.

• Z12029008GAS INFLATORS