Distributor intelligence · Global sourcing

Find the next medical-device opportunity — and the evidence to act on it.

IntelMed connects manufacturer, device, clinical, tender and safety records into one sourcing workspace, so distribution teams can move from market signal to defensible shortlist without losing the source trail.

Invitation-only access · Built for medical-device distribution and sourcing teams

Example sourcing brief

Portable diagnostic imaging

Illustrative category · Southeast Europe

Review now
Demand evidence
A relevant public tender has entered the market
Supplier context
Candidate manufacturers and devices are linked for review
Risk screen
Regulatory, clinical, recall and supply evidence stays visible

Recommended next step

Review supplier fit, territory rights and the live tender documents before acting.

Every recommendation keeps its citations and observation dates.

Live, source-backed coverage in this workspace

Companies mapped
55,385
Devices indexed
1,728,829
Regulatory records
3,377,513
Distributor markets
0

Connected market intelligence

One workspace for the whole sourcing question.

Finding a product is only the beginning. IntelMed keeps demand, readiness, risk and supplier context connected, so a promising signal can become a researched commercial decision instead of another browser tab.

Prioritise

Opportunity signals

A ranked inbox turns tender demand, clinical movement, regulatory changes, supply gaps and company events into specific next steps for your markets.

Investigate

Device intelligence

Search global device records by category, risk class, manufacturer country, market availability, specifications and linked clinical evidence.

Anticipate

Clinical pipeline

Track worldwide device studies, sponsors, sites, lifecycle changes and results to find emerging categories worth deeper diligence.

Validate demand

Tenders & procurement

See public buying activity, delivery markets, deadlines and device categories with a direct route back to the official notice.

Screen risk

Safety & supply

Keep FDA recalls, enforcement actions, shortages and discontinuances beside the product record—not in a separate research trail.

Build the shortlist

Company landscape

Connect manufacturers to devices, regulatory progress, markets, funding and distributor coverage before starting a conversation.

From signal to action

A sourcing process your team can repeat.

IntelMed is built around the decision a distributor needs to make—not around the shape of any single registry.

Evidence stays attached

Open the official record, see when IntelMed observed it, and distinguish a source fact from an inferred opportunity.

  1. 01

    Set the sourcing mandate

    Define the device categories, territories, regulatory threshold and commercial signals that matter to your distribution business.

  2. 02

    Investigate connected evidence

    Move from a ranked signal into the manufacturer, device, clinical, tender and safety context without rebuilding the research trail.

  3. 03

    Decide and keep watch

    Shortlist, dismiss or action the opportunity, then monitor the underlying evidence for changes that could alter the decision.

Provenance by design

Trace the decision back to the evidence.

Sourcing intelligence is only useful when your team can challenge it. IntelMed preserves the record behind each claim and makes uncertainty explicit.

  • Source names and identifiers stay visible beside the fact they support.
  • Observation dates make freshness inspectable instead of implied.
  • Registry evidence, platform inference and commercial verification remain distinct.

Regulatory & device

openFDA · AccessGUDID · EUDAMED

Clinical development

ClinicalTrials.gov · EU clinical investigation reports

Demand & procurement

TED — Tenders Electronic Daily · public procurement records

Safety & supply

FDA recalls · enforcement reports · shortages and discontinuances

IntelMed supports research and supplier discovery. It does not certify devices, establish distribution rights, confirm product availability or replace regulatory and commercial due diligence.

Manufacturer intelligence

See the company behind each signal.

Move from a market event to the manufacturer, its product portfolio and the regulatory evidence already on file. These are examples from the current IntelMed dataset.

STENTS

Greece

0 devices indexed

Profile evidence available in IntelMed

NVIDIA GmbH

Germany

0 devices indexed

Profile evidence available in IntelMed

BOOM

Greece

0 devices indexed

Profile evidence available in IntelMed

Texas Instruments, Inc.

United States

3 devices indexed

510(k) · Cleared

Your next sourcing decision

Build a medical-device shortlist you can defend.

Bring opportunity discovery, supplier research and source-level diligence into one shared workflow.

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Access is managed by invitation.