10001302

Organization name

Fidia Farmaceutici S.p.A.

SRN

IT-MF-000026988

Manufacturer status

Active

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

• CW999

  For cutaneous use only.
• CW999

  Do not use with products containing quaternary ammonium salts (for example benzalkonium chloride), which may alter the product.
• CW007

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

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

  EUDAMED did not publish a description for this code.
• CW999

  it should only be used once for a single patient and discarded after use.
• CW999

  Do not discard the empty packaging into the environment and dispose of according to applicable national guidelines.
• CW999

  Avoid contact with eyes. In case of contact with eyes, rinse with water.
• CW999

  Keep out of children’s reach and sight.
• CW999

  This product has not been tested in pregnant women, breast-feeding women or children.

Primary placement in Czechia; available across 2 countries total.

Trade name

not provided

UDI-DI code

D-100013022T

Basic UDI-DI

B-100013022T

Reference / catalog number

10001302

Issuing entity

EUDAMED

Risk category

Class IIa

Applicable legislation

MDD [Directive 93/42/EEC 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

• 10x10 cm
• 4
• 5x5 cm
• Apply every 48 hours

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

D-100013022T

DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.

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

• M0599MEDICAL PLASTERS - OTHER