pCON2-4-15-5

Organization name

phenox GmbH

SRN

DE-MF-000006524

Manufacturer status

Active

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

• CW265

  COBALT
• 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.
• CW026

  EUDAMED did not publish a description for this code.
• CW011

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

  The treatment is contraindicated for use in pa-tients for whom: - Antiplatelet and/or anticoagulation therapy is contraindicated. - Antiplatelet therapy did not start in a timely manner prior to treatment. - Antiplatelet and/or anticoagulation therapy (with e. g. acetylsalicylic acid, Clopidogrel, Prasugrel or Ticagrelor) was ineffective. - Angiography demonstrates the anatomic conditions are not appropriate for endovas-cular treatment.

Primary placement in Germany; available across 27 countries total.

Trade name

not provided

UDI-DI code

04260123784225

Basic UDI-DI

426012378BifurImplantGK

Reference / catalog number

pCON2-4-15-5

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

https://phenox.net/mdr/bai/

Clinical sizes

No clinical sizes registered for this device.

• P070402020102NON-STAINLESS STEEL PERIPHERAL VASCULAR BARE METAL STENTS

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