MRI implant safety platform

Implant safety information your MRI team can trust

When a patient has an implant, MRI teams need to identify the device, review the safety conditions, check the scanner context, apply local policy, and document what was checked. NordInsight brings that work into one clearer process.

Implant conditions are extracted from manufacturer IFUs, reviewed before publication, and tied back to the source — versioned, last-checked, and traceable for clinical use.

nordinsight.com / implant / linq-ii
NordInsight implant detail page — LINQ II, showing source IFU, MRI Code, version history, last-checked date, department approval, and MR conditions
Human-validated implant data
Conditions are extracted and checked by people, not generated by AI.
Source-backed IFUs
Manufacturer IFUs are hosted, linked, and versioned for traceability.
Built for department workflows
Policies, scanners, approvals, reports, and CPT documentation live together.
The real workflow

MRI safety work is not just looking up an implant

When a patient has an implant, MRI teams need to find device details from partial information, locate the right manufacturer documentation, interpret scan conditions, check whether local policy applies, confirm scanner compatibility, and document the decision.

That work is often done while the patient is waiting, the schedule is under pressure, and the team needs an answer they can stand behind. NordInsight is built around the full MRI implant safety workflow, from device identification to clear documentation.

Find implants when the patient only has partial information
Verify conditions against the manufacturer IFU
Check field strength, coils, SAR/B1+rms, scan region, and scanner limits
See whether the implant has already been approved locally
Follow department protocols and escalation pathways
Document the work for clinical review, auditability, and CPT reporting
FROM PATIENT ARRIVAL TO CLEAR DOCUMENTATION
01
Patient arrives
Often with partial implant info
02
Device ID
Identify the exact device
03
IFU verification
Confirm against the source
04
Scanner check
Fit to local equipment
05
Approve / escalate
Apply department policy
06
Document
Report & CPT record
Trust & validation

Human-reviewed and source-backed

Implant conditions are read and checked by people.

Implant safety conditions are read from the manufacturer IFU by trained staff and checked before they are published.

Every condition is tied back to the original source document. Version history, last-checked dates, and change tracking help departments understand what information was used at the time of review.

01
Manufacturer IFU
The original source document
02
Human review
Conditions read by trained staff
03
Review & validation
Checked before publication
04
Published source-backed
With IFU, version history, and last-checked date
Implant conditions are extracted from manufacturer IFUs
Data is reviewed before publication
Source documentation is attached
Version history is preserved
Last-checked dates are visible
Department approvals can be removed if conditions change
Source-backed implant pages

Every implant page is built for traceability

NordInsight implant pages are designed so teams can verify where the information came from and understand how it has changed over time.

01

Source IFUs attached

Manufacturer documentation is linked directly from the implant page.

02

Version history

Teams can see when implant information changes, and what changed.

03

Last checked

Clear timestamps help users judge how fresh the information is.

04

MRI Codes

Short codes document the device and lead back to the current page.

Static printouts age. MRI Codes stay connected.

NordInsight assigns a short MRI Code to each implant so staff can document the device without copying static conditions that may become outdated. When the code is searched later, it leads back to the current source-backed implant page.

MRI Code
NI-7F4K2
Resolves to current conditions
Survives IFU revisions
Printable on the patient record
Department governance

Turn repeated implant reviews into department knowledge

MRI teams often review the same implants repeatedly. NordInsight helps departments standardize that work without losing control. When conditions change, NordInsight can remove the approval and notify the team so the device is reviewed again.

Change-aware approval lifecycle
01
Reviewed by department
A local expert evaluates the device
02
Approved for site
Visible in the workflow
03
Conditions change
Source IFU is updated
04
Approval removed
Team is notified automatically
05
Re-review
Device is checked again
Department approvals
Mark implants reviewed and approved for local use.
Approval history
See who approved an implant, and when.
Change-aware
Approvals can be flagged or removed when source conditions change, so the device is reviewed again.
Multi-site support
Different scanners and workflows across locations.
nordinsight.com / scanner / room-44
NordInsight scanner compatibility — Room 44 photo with a caution that patient positioning may affect the spatial gradient limit, the implant's 3.3 T/m maximum, and a table of the scanner's static field, spatial gradient at 40–70 cm, and maximum slew rate
Implant spatial-gradient limit checked against the real scanner — room photo, field strength, per-distance gradients, and slew rate.
Scanner compatibility

Check conditions against the scanners your team actually uses

MRI safety decisions depend on the scanner, not just the implant. Add MRI rooms, scanner models, coils, spatial gradient information, and local notes so staff can check whether implant conditions fit the equipment at each site.

Scanner-specific checks

Compare against field strength, model, coils, and local equipment.

Room-level context

Organize scanner information by room or site.

Local notes

Department-specific scanner notes and operational guidance.

Compatibility warnings

Highlight where conditions may not match available equipment.

Protocols & local guidance

Keep implant guidance, local SOPs, and safety resources in the same workflow

MRI safety depends on local practice as well as manufacturer documentation. Keep local protocols, escalation pathways, scanner notes, training videos, reference links, and implant-specific instructions searchable alongside implant information.

Local protocols

Department-specific MRI safety workflows and escalation steps.

Searchable guidance

Internal guidance is easy to find during the clinical workflow.

Implant-specific notes

Attach local instructions to specific devices or categories.

Training resources

Videos, links, documents, and reference material for staff.

nordinsight.com / policies
NordInsight department policies — a searchable, tag-filtered table of MRI safety policies and SOPs showing title, tags, author, and updated/effective/expiry dates with draft, completed, expired and pending-approval tabs
Department policies and SOPs — searchable, tagged, with author, effective and expiry dates, alongside implants.
Documentation & CPT

Document implant safety work clearly

Implant safety work takes time — reviewing IFUs, evaluating conditions, coordinating with radiologists, contacting outside facilities, preparing patients, and documenting decisions. NordInsight helps make that work visible, and supports CPT reporting for US teams.

Report generation

Structured MRI safety reports built from implant information.

Source references

Include IFUs and supporting documentation in the report.

Time logs

Record time spent on implant review and preparation.

CPT eligibility tracking

Track whether the work may support CPT reporting.

NordInsight supports documentation and eligibility tracking. It does not determine reimbursement or guarantee payment.
nordinsight.com / case / preview
NordInsight case workspace preview — a printable MRI safety report showing case context, implants and foreign bodies, full MRI conditions for the InterStim neurostimulator, an applicable CPT codes section, and a signing-QHP risk-benefit option
Case workspace preview — context, implants, MRI conditions, applicable CPT codes, and optional signing-QHP risk-benefit analysis, ready to print or copy.
Active implant builder
Spinal cord stimulation systemBeta
System
Select…Nevro · Senza SCS System
Generator
Select…NIPG1000 · Senza IPG
Leads
Select leads…LEAD1058-xx(B)LEAD2008-xx(B)
Resulting MR conditionsMR Conditional
Static magnetic field
Operating mode
Max SAR / B1+rms
Scan region
Matched to this exact generator + lead build.
Identify the system, generator and leads — NordInsight resolves the conditions for that exact build, instead of working through every IFU combination by hand.
Active implants

Make complex active implant conditions easier to review

Active implants often require interpreting long IFUs with generator, lead, field strength, scan region, and manufacturer-specific dependencies. NordInsight helps teams select system components and view the relevant MRI conditions directly.

Generator & lead workflows

Support complex device combinations.

Field & scan-region context

Surface conditions for the relevant scan setup.

Checklist-style prep

Follow required steps before scanning.

Hybrid-system support

Reason through exchanged leads and mixed systems.

Built with real teams

Built with real MRI safety teams

NordInsight is developed with feedback from MRI technologists, MRSOs, MRMDs, radiologists, imaging leaders, and hospital teams working with implant safety, documentation, and reimbursement workflows.

NordInsight is shaped around the practical workflow of the teams responsible for MRI safety decisions every day.

15–20min
Saved per implant in one Northern California case study versus the team's previous implant information workflow.
Human support
Direct support from the NordInsight team, not a chatbot.
Traceable data model
Information tied to source documentation, version history, and last-checked dates.
Built with input from technologists, safety officers, radiologists, imaging leaders, and revenue-cycle stakeholders.
Trust checklist

Trust is a product feature

NordInsight is designed around the controls MRI teams need when implant safety information affects real clinical decisions.

Trust mechanism
Why it matters
Human-reviewed implant conditions
Reduces reliance on unverified extraction.
Source IFUs attached
Lets teams verify the original manufacturer documentation
Version history
Shows what changed over time
Last-checked dates
Helps users judge information freshness
Department approvals
Standardizes safe local decisions
Approval removal on condition change
Prevents stale approvals
Scanner-specific context
Helps match conditions to available equipment
Local protocols and guidance
Keeps department workflows accessible
Report-level audit trail
Supports accountability and review
Professional sign-off
Supports clear accountability and review.
CPT time logs and source references
Makes implant safety work visible and defensible
Book a demo

See how NordInsight works with your MRI safety workflow

Bring one difficult implant workflow, one local protocol, or one CPT reporting example. We'll show how NordInsight would support your team's actual process.

NordInsight

The MRI safety platform for teams that need speed, but cannot compromise on trust.

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Implant databaseScanner compatibilityProtocols & guidanceCPT reporting
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© 2026 NordInsight. Source-backed MRI safety information built for clinical use.Implant conditions are human-validated, not AI-generated.