BATCH TRACKING FOR MEDICAL & LAB SUPPLIES

Expiry Management for Medical & Lab Supplies — Audit-Ready, Error-Free

TraceLot automates FEFO allocation, blocks expired inventory, and maintains the lot-level traceability FDA and ISO standards require — fully synced with Veeqo.

TraceLot dashboard showing medical supply batch tracking with expiry dates and compliance status

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The Problem

Why Medical & Lab Supply Distributors Need Automated Batch Tracking

Pain Point

Critical Expiry Accuracy

Expired reagents produce invalid test results. Expired medical supplies create patient safety risks. In medical and lab contexts, expiry accuracy isn't optional — it's critical.

Pain Point

High-Value Inventory Write-Offs

Reagents, test kits, and medical supplies are expensive. Without FEFO automation, newer stock ships while older batches expire — destroying significant inventory value.

Pain Point

FDA and ISO Documentation Requirements

Medical device regulations and ISO 13485 require documented batch traceability. GLP and CLIA standards mandate reagent lot tracking. Spreadsheets can't meet these requirements reliably.

Pain Point

Lot Recall Complexity

When a manufacturer issues a lot recall, can you identify every lab or facility that received affected products immediately? Manual tracking delays critical safety responses.

The Solution

How TraceLot Protects Medical & Lab Supply Operations

Solution

Automatic FEFO on Every Order

Every order automatically receives the earliest-expiring batch. Your team sees exact lot numbers in Veeqo — ensuring labs and facilities receive products with maximum remaining shelf life.

Solution

Expiry Firewall

Expired medical supplies and reagents are automatically blocked from Veeqo inventory. No expired products can be sold, protecting patient safety and test validity.

Solution

FDA & ISO-Ready Traceability

Maintain complete lot-level records for FDA medical device requirements, ISO 13485, and laboratory standards. Full batch history from manufacturer through customer.

Solution

Instant Recall Capability

Generate a complete list of affected customers by manufacturer lot number in minutes. Respond to FDA recalls and safety alerts immediately.

Ready to streamline your medical & lab supplies inventory?

Join hundreds of medical & lab supplies businesses already using TraceLot to eliminate expired shipments and stay compliant.

Regulatory Compliance

Built for Medical & Laboratory Standards

Medical devices, lab reagents, and supplies face rigorous regulatory requirements. TraceLot provides compliant batch traceability infrastructure.

Regulation

FDA Medical Device (21 CFR Part 820)

Quality System Regulation requires documented batch control and distribution records.

  • Lot-level traceability
  • Distribution records
  • Expiry documentation
  • Recall response capability

Regulation

ISO 13485 Quality Management

Medical device quality standards require documented batch tracking. TraceLot helps maintain the traceability records needed.

  • Batch identification
  • Traceability records
  • Distribution documentation
  • Audit-ready batch history

Regulation

Laboratory Standards (GLP, CLIA, CAP)

Laboratory regulations require reagent lot tracking and expiry management.

  • Reagent lot documentation
  • Expiry tracking
  • Calibrator/control lot records
  • Chain of custody

Results Medical & Lab Distributors Achieve with TraceLot

0

Expired products shipped

100%

Lot traceability

<5 min

Recall report generation

Audit

Ready at all times

How It Works

Get Started in 10 Minutes

1

Connect Veeqo

Link your Veeqo account with OAuth in 2 minutes. No code, no IT support needed.

2

Add Batches

Add batches with manufacturer lot numbers and expiry dates. Track calibration dates, storage requirements, and certification information as needed.

3

Ship with Confidence

TraceLot auto-assigns FEFO batches to every order. Expired products are blocked automatically. Labs receive products with maximum usable life.

Comparison

Manual Tracking vs TraceLot

CapabilityManual TrackingWith TraceLot
Batch Tracking
Error-prone spreadsheets
Automated batch assignment
FEFO Allocation
Manual picker instructions
Automatic on every order
Expired Stock Protection
Risk of shipping expired medical and lab products
Expiry Firewall blocks automatically
FDA/ISO Records
Documentation gaps, audit risk
Complete regulatory-ready records
Recall Readiness
Days to trace affected orders
5-minute batch-to-customer report
Veeqo Integration
Manual reconciliation
Two-way sync, zero double-entry

FAQ

Medical & Lab Supply Tracking Questions

How does TraceLot help with FDA medical device distribution requirements?
TraceLot maintains the distribution records that FDA's Quality System Regulation requires. Every lot is tracked from receipt through customer shipment with complete documentation for audits and recalls.
Yes. TraceLot tracks manufacturer lot numbers, expiry dates, and distribution to laboratory customers. This supports GLP, CLIA, and CAP requirements for reagent lot documentation.
TraceLot lets you instantly identify every customer who received the recalled lot. Generate a report in minutes and notify affected facilities immediately, meeting FDA recall requirements.
TraceLot provides batch identification and traceability records that support ISO 13485 requirements. All lot movements are logged automatically, helping you maintain the documentation needed for quality audits.
Yes. You can add storage requirements, handling notes, and special conditions to batch records. This information is available for warehouse staff and quality documentation.

Protect Patient Safety with Proper Expiry Management

Join medical and lab supply distributors using TraceLot to automate FEFO, stay compliant, and never ship expired products.

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