Exchange set for percutan. nephrostomy

Organization name

Teleflex Medical

SRN

IE-MF-000015868

Manufacturer status

Active

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

• CW999

  Single use: Do not reuse, reprocess or resterilize. Reuse of device creates a potential risk of serious injury and/or infection which may lead to death. Reprocessing of medical devices intended for single use only may result in degraded performance or a loss of functionality. Each device set is supplied in an individual sterile pouch. The device and its components are guaranteed sterile unless the unit packaging has been opened or damaged, but no longer than stated on the label.
• CW999

  Do not resterilize
• CW999

  Do not use if package is damaged
• CW999

  Do not re-use
• CW999

  Consult instructions for use
• CW999

  MR SAFE

Primary placement in Ireland; available across 22 countries total.

Trade name

Exchange set for percutan. nephrostomy

UDI-DI code

14026704728456

Basic UDI-DI

08019020000000000000252KM

Reference / catalog number

340014-000060

Issuing entity

GS1

Risk category

Class IIa

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

No clinical sizes registered for this device.

• U040299DEVICES FOR PERCUTANEOUS NEPHROSTOMY - OTHER

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