2110403084

Organization name

Aurora Srl

SRN

IT-MF-000018589

Manufacturer status

Active

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

• CW011

  The use of fire requires the utmost care: protect your hair and face adequately from the flame. Carry out the treatment only with the assistance of an adult person, in a place free from draughts and away from flammable substances and/or objects. Do not use in the event of any pathology in the otological area, recent surgery or allergy to the components of the product.
• CW009

  EUDAMED did not publish a description for this code.
• CW030

  EUDAMED did not publish a description for this code.
• CW010

  EUDAMED did not publish a description for this code.
• CW007

  EUDAMED did not publish a description for this code.
• CW032

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

  EUDAMED did not publish a description for this code.
• CW059

  EUDAMED did not publish a description for this code.
• CW135

  EUDAMED did not publish a description for this code.
• CW138

  EUDAMED did not publish a description for this code.
• CW277

  EUDAMED did not publish a description for this code.

Primary placement in Spain; available across 1 country total.

Trade name

not provided

UDI-DI code

08017690000090

Basic UDI-DI

8017690CONESX6

Reference / catalog number

2110403084

Issuing entity

GS1

Risk category

Class I

Applicable legislation

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

Status

On the market

Quantity

2

Additional product description

—

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.

• Q0399ENT DEVICES - OTHER