AS/NZS 5369 Audit-Ready • TGA Compliant • ADA-Aligned
Exclusive distributor of ALPRO Medical GmbH in Australia and New Zealand
Contact
Home
Resource centreDocumentsTraining centre Compliance Research About us Contact
flowing.
Decontamination of procedural water

i3 FIVE

flowing.

Higher-flow inline filtration.

For specified equipment applications, including reprocessing. Stated flow: 20 L/min at 5 bar.

i3 FIVE

Key facts

why practices choose i3 five.

  • High-flow 0.2 µm microfiltration, sterile filtration acc. ASTM F8381
  • 50 days (7 weeks) of operation1
  • Quick-release coupling for fast, documented filter changes1
  • Wipe-disinfectable housing1

In practice

in the loop.

i3 FIVE — Schematic — the i3 FIVE inline filter installed in the inflow of an automatic endoscope reprocessor
Installed inline at the reprocessing-machine inlet via a quick-release coupling — a barrier against waterborne microbes at the pre-cleaning and final-rinse stages.

Product information

the essentials.

With the i3 FIVE inline sterile filter, Biodegree offers a solution where safe microfiltration of waterborne pathogens is needed at high water flows — for example the automatic reprocessing of medical devices such as endoscopes, and filling birthing tubs. It provides sterile filtration of tap water in the inflow pipes of devices and instruments.

Key Features

  • High-flow 0.2 µm microfiltration; sterile filtration acc. to ASTM F838.
  • 50 days (7 weeks) operating time with a high, stable flow rate.
  • Wipe-disinfectable filter surface.
  • Safe, quick connection by quick-release coupling.
  • Versatile high-flow use — endoscope washer-disinfectors and filling birthing tubs.
Membrane
0.2 µm high-performance flat membrane (microfiltration); sterile filtration acc. to ASTM F838; bacterial retention > 7 log/cm² B. diminuta (manufacturer data). Material not stated — see the data sheet.
Mounting
Installed inline at the reprocessing-machine inlet via a quick-release coupling; a barrier at the pre-cleaning and final-rinse stages. Wipe-disinfectable housing. Document changes with the i3 trackApp / change service. Do not install in tankless low-pressure systems; filtration does not change dissolved chemical content.
Field of application
High-flow inline sterile filtration for high-water-flow settings — automatic reprocessing of medical devices (e.g. endoscopes), pre-cleaning and final-rinse stages, and filling birthing tubs.
Clinical data & approvals
Used in line with DIN EN ISO 15883 (washer-disinfector standard); sterile filtration acc. ASTM F838; plastics suitable for use with drinking water to BS 6920 (manufacturer data). Not ARTG-registered.
Service life
50 days (7 weeks), high stable flow. Operating temperature 60 °C (up to 70 °C for 30 min); max 5 bar; initial flow 20 L/min at 5 bar (manufacturer data).
Delivery forms
Ordered in Australia through Biodegree via i3 Membrane — ask Biodegree for the current order code.
Sterile filtration · ASTM F838ISO 15883 reprocessing

Figures are manufacturer / EU data, not an Australian therapeutic claim; not ARTG-registered. Follow the data sheet and IFU.

Documents

docs &
downloads.

Need a document that is not listed? Speak to Biodegree — we supply current Product Information (PI), Instructions for Use (IFU) and scientific / test documentation on request.

FAQ

common
questions.

What is the i3 FIVE and where does it fit?

The i3 FIVE is a high-flow inline 0.2 µm sterile filter for the inflow pipes of water-injected devices and instruments. It suits high-water-flow settings — the automatic reprocessing of medical devices such as endoscopes, pre-cleaning and final-rinse stages, and filling birthing tubs — as a barrier against waterborne pathogens such as Legionella pneumophila, Pseudomonas aeruginosa and mycobacteria.

How fine is the i3 FIVE membrane and what does it retain?

The i3 FIVE uses a high-performance flat membrane with a nominal pore size of 0.2 µm (microfiltration). Manufacturer data states bacterial retention of more than 7 log per cm² for Brevundimonas diminuta (bacterial retention to ASTM F838). These are manufacturer figures.

How long does an i3 FIVE last?

The service life is 50 days (7 weeks), with a high, stable flow across that period. Document each change with the i3 trackApp.

What is the flow rate?

Manufacturer data states an initial flow of 20 L/min at 5 bar — the highest in the i3 range — with a maximum operating pressure of 5 bar (operating temperature 60 °C, up to 70 °C for 30 minutes).

How is the i3 FIVE installed and used for reprocessing?

It fits inline at the machine inlet with a quick-release coupling and serves as a barrier at the pre-cleaning and final-rinse stages. The housing is wipe-disinfectable. Manufacturer data states it is used in line with DIN EN ISO 15883, the washer-disinfector standard.

What standards does the i3 FIVE meet, and how is it ordered?

Manufacturer data references DIN EN ISO 15883 for reprocessing and ASTM F838 for bacterial retention, and states the plastics are suitable for use with drinking water to BS 6920. In Australia the i3 FIVE is ordered through Biodegree via i3 Membrane — ask Biodegree for the current order code.

Sustainability

Fully biodegradable. Free from aldehydes and phenols.

Every Alpro formula is designed to break down and return to nature in diluted form — no aldehydes, no phenols, no chlorine, and no silver ions or metals in our waterline care. And every product is made in Germany, in an emission-free facility powered by solar and geothermal energy.

More about Alpro

What's next?

i3 ONE

  1. i3 ONEREF · 3582
  2. i3 TWO
  3. i3 FOURREF · 3586
  4. i3 FIVE
i3 ONE
i3 sterile filtration

i3 ONE

REF · 3582

Compact legionella filter for the tap

Learn more

Get help

not sure what
your practice needs?

Tell us your setup and we'll match the right protocol, zone by zone.

Get help
  • Exclusive AU & NZ distributor
  • Source-verified documentation
  • Contact the Biodegree team

Customer service & support

help &
support.

Get help with your product, find the documents, or open the customer service portal.

Resource centre

Product documents and help, together.

Find resources, ask a question or prepare an enquiry. No account needed.

Disclaimers

  1. Efficacy, contact-time and composition figures are as stated on the manufacturer Product Information or in the cited study (manufacturer/study-stated) — verify before external or clinical use.