Crush and Mix...
Safely.

Portable, Disposable, Closed-Chamber Pill Crushing and Mixing Device

Engineered to support safer crushing, mixing, and dose withdrawal of oral medications through a contained, single-use workflow.

Crush and Mix...
Safely

Portable, Disposable, Closed-Chamber Pill Crushing and Mixing Device

Engineered to support safer crushing, mixing, and dose withdrawal of oral medications through a contained, single-use workflow.

What is EnOPrep?

EnOPrep is a single-use closed-chamber pill crushing and mixing device designed for point-of-care crushing, mixing, and dose withdrawal of solid oral medications for oral and enteral administration.

Its integrated workflow combines tablet crushing, suspension preparation, and medication withdrawal into one contained process to support efficient bedside preparation while helping reduce environmental powder dispersion associated with traditional crushing
methods.

Advancing Medication Safety for Patients and Healthcare Workers — One Pill at a Time.

Pain Points of Standard Pill Crushers

  • Crushing medications leads to airborne powder particles and contamination.
  • PPE must be worn to safely crush medications and mix into solution.
  • Bulky crushing devices are not portable for point of care use.
  • BCMA compliance is decreased due to opening medications outside the point of care.
  • Reusable pill crushers leads to cross contamination risks.
  • Separate reusable pill crushers for hazardous use and non-hazardous use must be maintained and labeled.
  • Hard to crush pills result in poor consistency of final drug product.
  • A large percentage of the medication dose can be lost due to improper crushing and mixing.

EnOPrep's Solution

Closed-Chamber Design:

Features a sealed internal crushing chamber with filter-assisted air venting designed to help contain powder during crushing and mixing.

High Yield

Bench testing demonstrated up to 98% yield during crushing, mixing, and withdrawal.

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Exposure-Reducing Workflow

Designed to help reduce environmental contamination associated with traditional open pill crushing methods.

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Point-of-Care Ready:

Portable design supports bedside medication preparation and barcode medication administration workflows.

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 Single-Use Design:

Disposable device helps reduce cleaning burden and cross-contamination risk.

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Safety

EnOPrep’s closed-chamber design helps reduce environmental powder dispersion during tablet crushing and mixing compared with traditional open crushing methods. Its contained workflow supports safer preparation of hazardous and high-risk oral medications at the point of care.

Efficiency

EnOPrep streamlines crushing, mixing, and dose withdrawal into a single-use workflow, reducing preparation steps and supporting efficient bedside medication preparation when crushing is clinically appropriate.

Reliability

Engineered crushing teeth and integrated suspension preparation are designed to produce consistent particle reduction and uniform mixing to support accurate dose preparation and high medication recovery.

Crush and Mix...Safely

Performance Highlights

  • Up to 98% Yield – Demonstrated in bench testing during crushing, mixing, and withdrawal
  • Closed-Chamber Workflow – Designed to help reduce powder dispersion during medication preparation
  • Single-Use Disposable Design – Helps minimize cleaning burden and cross-contamination risk
  • ENFit-Compatible Connection – Supports compatibility with standard enteral syringe workflows
  • Point-of-Care Ready – Portable design supports bedside medication preparation and administration workflows

Crush. Mix. Dispense.

Frequently Asked Questions

No. EnOPrep is not a Closed System Transfer Device (CSTD).

EnOPrep is classified as a Class I FDA-registered pill crushing and mixing device and is designed as a closed-chamber system for crushing and mixing oral solid medications. It is not intended to replace CSTDs where such devices are required for sterile compounding or drug administration workflows.

Yes! EnOPrep can safely be disposed of after use. No more clean up and potential cross contamination.

After completion of the dose preparation you can easily administer the solution enterally or orally.

No! EnOPrep has a wide range of markets including home health care, hospice, long term care, and veterinary.

EnOPrep meets the definition for being a protective medical device and prevents aerosolization of the crushed drug (USP <800> compliant).

This device is registered with the FDA as a Class I medical device and is available for patient use in accordance with applicable regulatory requirements.