We have organised IPD Instructions for Use by the actual product group so that the general prosthetic instructions, ScanLogiQ, NT-Line, torque wrench and Implant Card documentation are not mixed together.
First identify the product group. The revision number in the title is not cosmetic: it tells you which version of the documentation you are reading.
Ti-base, abutment, fixation screw, Custom Interface, CEREC® or IPDmilled → start with the main “Abutments and accessories” instructions.
General instruments → instrument instructions. ScanLogiQ, NT-Line and the torque wrench each have their own separate documents.
The Implant Card has its own instructions. We list the Rev. 03 brochure separately below because it is not an Instructions for Use document.
Each card shows the specific revision and date. Click to open the local PDF; the second link always leads to the manufacturer’s official documentation to verify that the revision is current.
Rev. 07 · 14 Jan 2026 · English
Main instructions for IPD prosthetic components. They describe intended use, compatibility and reference structure and include, among other branches, Custom Interface, CEREC® Ti-bases and IPDmilled.
Rev. 07 · 25 Mar 2025 · English
Instructions for instruments and laboratory accessories used with IPD implants and abutments. They help distinguish clinical from laboratory use and locate product ranges by reference code.
Rev. 01 · 12 Jan 2026 · English
Dedicated Instructions for Use for the ScanLogiQ Kit. They distinguish Scan Flag iQ, One Shot iQ, Reverse iQ, Control Plate iQ and other kit components and describe digital transfer of the position of multiple implants or MUA using an intraoral scanner.
Rev. 02 · 9 Dec 2024 · English
Instructions for the separate IPD NT-Line product branch. They cover its reference logic, compatible systems and laboratory/digital components, including DIM analogs.
Rev. 02 · 18 Apr 2023 · English
Specific instructions for the IPD/DI-00-90 contra-angle torque wrench. They describe adapter replacement, correct activation of the set torque, limitations of use and cleaning and sterilisation requirements.
Rev. 02 · 13 Apr 2023 · English
One-page instructions for completing the Implant Card. They explain the information added by the healthcare provider and the role of the card in identification and traceability of implanted components.
We distinguish supplementary documents from Instructions for Use so that a higher revision number is not mistaken for an automatically “newer IFU” serving the same purpose.
The brochure dated 13 Dec 2024 summarises the purpose of the Implant Card, information on its front and back and the symbols used. For the actual “Implant Card Instructions for Use”, we use Rev. 02 above.
The FAQ focuses on selecting the document and revision, not on replacing the manufacturer’s technical instructions themselves.
Start with the “IPD Abutments and accessories” document. This is the main prosthetic Instructions for Use. For specialised product branches such as ScanLogiQ or NT-Line, use their dedicated instructions.
This page highlights the latest revisions in the supplied English documentation. Before clinical use, however, we recommend checking the current status in the official IPD documentation as well, because the manufacturer may publish a new revision before the local copy is updated.
The archive supports document traceability and retrospective verification of which version was available at a given time. A historical revision must not replace the current Instructions for Use.
ScanLogiQ has its own dedicated Instructions for Use in the supplied documentation. We therefore show it separately to avoid confusion with the general instructions for instruments and laboratory accessories.
They explain which information is added to the card by the healthcare provider and how the card supports identification and traceability of implanted components.
No. The supplied file is labelled as a brochure, not as “Instructions for Use”. We therefore list it separately as a supplementary document and highlight Rev. 02 dated 13 Apr 2023 as the Implant Card Instructions for Use.
Send us the IPD reference or a photograph of the label. We can identify the product group and direct you to the corresponding current instructions.
No. The local English PDF provides convenient access to the documentation, but the official IPD documentation remains the reference point for verifying the latest published revision.
Send us the IPD code or a photograph of the label. We will identify the correct product group and current document.
IFU means Instructions for UseInstructions for Use. eIFU is an Instructions for Use document published electronically. On the English website we therefore primarily use the clear label Instructions for use; the IFU/eIFU abbreviation is retained where it helps match the manufacturer’s terminology and document searches.
