05993023096318

Trade name

not provided

UDI-DI code

05993023096318

Basic UDI-DI

599302677ADYN

Reference / catalog number

05993023096318

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

—

Additional information URL

https://www.medicontur.com/eifus

Clinical sizes

• 29.5 MU104
• 0 MU104
• 6 MU50
• 13 MU50

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

• P030102090202IOLs, APHAKIC, MONOFOCAL, ASPHERIC, HYDROPHILIC ACRYLIC

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

• CW001

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

  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.
• CW011

  EUDAMED did not publish a description for this code.