Main information

  • Trade name:
  • Ambix Intraport T Powerflow - Port, infusion, implantable
  • Class:
  • Class III
  • Medicine domain:
  • Humans
  • Medicine type:
  • Medical device



  • Available in:
  • Ambix Intraport T Powerflow - Port, infusion, implantable
  • Language:
  • English

Other information


  • Source:
  • Dept. of Health,Therapeutic Goods Administration - Australia
  • Authorization number:
  • 222677
  • Last update:
  • 08-10-2017

Public Assessment Report

Public Summary

Summary for ARTG Entry:


Fresenius Kabi Australia Pty Limited - Ambix Intraport T Powerflow - Port, infusion, implantable

ARTG entry for

Medical Device Included Class III


Fresenius Kabi Australia Pty Ltd

Postal Address

Level 2, 2 Woodland Way,Mount Kuring-gai, NSW, 2080


ARTG Start Date


Product category

Medical Device Class III



Approval area

Medical Devices


- The inclusion of the kind of device in the ARTG is subject to compliance with all conditions placed or imposed on the ARTG entry. Refer Part 4-5,

Division 2 (Conditions) of the Therapeutic Goods Act 1989 and Part 5, Division 5.2 (Conditions) of the Therapeutic Goods (Medical Devices) Regulations

2002 for relevant information.

- Breaching conditions of the inclusion related to the device of the kind may lead to suspension or cancellation of the ARTG entry; may be a criminal

offence; and civil penalties may apply.




Fresenius Kabi AG

Else-Kroner-strasse 1

Bad Homburg, , D-61346



1. Ambix Intraport T Powerflow - Port, infusion, implantable

Product Type

Procedure Pack

Effective date



35911 Port, infusion, implantable

Functional description

Completely implantable catheter system consisting of a titanium casing, a medicine compartment with a

silicone membrane and a polyurethane catheter which can be connected to the port casing.

Intended purpose

Indicated when treatments require long-term, repeated access to the venous vascular system. Medicines,

intravenous infusions, parenteral nutrition or blood products, for example, can be applied via the venous

port systems. Also suitable for blood sampling purposes and high-pressure injection/infusion.

Variant information

Nil variant (as 1 device) -

Specific Conditions

No Specific Conditions included on Record

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Public Summary

Page 1 of

Produced at 02.12.2017 at 04:12:31 AEDT

This is not an ARTG Certificate document.

The onus is on the reader to verify the current accuracy of the information on the document subsequent to the date shown.

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