ITF001/c2

Organization name

Italfarmacia srl

SRN

IT-MF-000013116

Manufacturer status

Active

Certificate health across this manufacturer's portfolio.

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

• CW001

  EUDAMED did not publish a description for this code.
• CW009

  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.
• CW277

  EUDAMED did not publish a description for this code.

Primary placement in Italy; available across 1 country total.

Trade name

not provided

UDI-DI code

08055715332337

Basic UDI-DI

805571533ITF0018V

Reference / catalog number

ITF001/c2

Issuing entity

GS1

Risk category

Class III

Applicable legislation

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

Status

On the market

Quantity

3

Additional product description

Filling and modelling solution for the dermal matrix based on hyaluronic acid and amino acids. Description MY DERMA VISO is an injectable, sterile and apyrogenic medical device to be used for intradermal microinjection, which degrades slowly after implantation. Composition Hyaluronic acid sodium salt, L-isoleucine, L-leucine, L-lysine hydrochloride, L-proline, L-valine, glycine, L-serine, L-alanine, L-cysteine, phosphate buffer system, WFI-grade water. Packaging contents 3 vials of 5 ml for intradermal use - information sheet - adhesive labels for traceability. Indications MY DERMA VISO is indicated in the prevention and treatment of facial skin damage, such as dehydration, pigmentation

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.

• P900402RESORBABLE FILLING AND RECONSTRUCTION DEVICES