PRE-4-20

Organization name

phenox GmbH

SRN

DE-MF-000006524

Manufacturer status

Active

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

• CW011

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

  EUDAMED did not publish a description for this code.
• 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.
• CW265

  Cobalt
• CW999

  The use of the medical device group Thrombectomy Systems is contraindicated in patients with - preexisting hemorrhage in the brain tissue supplied by the target vessel and - established infarction in the brain tissue supplied by the target vessel.

Primary placement in Germany; available across 27 countries total.

Trade name

not provided

UDI-DI code

04260123784058

Basic UDI-DI

426012378ThrombectomyF6

Reference / catalog number

PRE-4-20

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/international/mdr/ts

Clinical sizes

No clinical sizes registered for this device.

• C010402020702MECHANICAL PERIPHERAL THROMBECTOMY AND THROMBOASPIRATION SYSTEMS

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

Certificate health across this manufacturer's portfolio.