ACCERO Stent

Trade name

ACCERO Stent

UDI-DI code

04260650332241

Basic UDI-DI

426065033ACCEROWF

Reference / catalog number

01-000803

Issuing entity

GS1

Risk category

Class III

Applicable legislation

MDR [Regulation (EU) 2017/745 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

• 3 MU50
• 10 MU50

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

• P0799VASCULAR AND CARDIAC PROSTHESES - OTHER

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

• CW009

  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.
• CW001

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

  EUDAMED did not publish a description for this code.

No certificate specifically references this device's Basic UDI-DI.