Mix2Vial® Transfer Device for Drug Reconstitution and Administration
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Mix2Vial® Transfer Device

Simplified vial-to-vial transfer for injectable drug preparation

Overview

Mix2Vial® Transfer Device Benefits

1

Simplified Reconstitution Workflow

Pre-assembled dual-spike design connects diluent and drug vials directly eliminating separate needle handling and streamlining preparation steps.

2

Supports Consistent Dose Preparation

Designed for reliable mixing and diluent transfer with efficient fluid pathway in fixed-volume systems that are suitable for biologics and specialty therapies.

3

Needle-Free Access

Reduces handling of sharps during vial connection supporting patient and caregiver training programs.

4

Designed for Stability and Control

Stable connection between vials during transfer supporting a consistent solvent flow into lyophilized drug vials and promoting reliable reconstitution across care settings.

5

Regulatory Confidence

Integrated into combination product kits globally, the Mix2Vial® transfer device offers additional confidence with applicable 510(k) clearance and CE-marking.

6

Applicable for Clinical and Self-Administration

Widely integrated into pharmaceutical kits and therapy programs, the Mix2Vial® transfer device supports both clinical and self-administration environments.*

Download the Mix2Vial® Transfer Device Info Sheet

Technical Information

Container Closure Integrity Testing

Sterilization

Mix2Vial transfer device is sterilized using Gamma irradiation.

Container Closure Integrity Testing

Materials of Construction

Mix2Vial transfer device is primarily constructed from medical‑grade polycarbonate. Additional materials may be used within the device assembly depending on configuration. A detailed materials list is available upon request.

Container Closure Integrity Testing

Shelf‑Life

Validated shelf‑life of 5 years. Check with our experts to confirm based on your configuration needs.

Which Device is right for your application?

ProductPrimary Use Case Drug FormDiluent Connection Target Key Benefits
Vial AdapterVial → Syringe transferLiquid or Lyophilized Prefilled syringe Luer syringe Needle‑free access; reduced preparation variability; vented and filtered configuration options
Mix2Vial® Transfer DeviceVial → Vial reconstitution Lyophilized VialVialSimple fixed‑volume transfer; intuitive snap‑fit design; easy‑to‑use reconstitution
MixJect® Transfer Device Vial → Syringe preparation Lyophilized Prefilled syringe Integrated syringe Integrated body and core design; supports needle‑based delivery; available in 13 mm and 20 mm formats
Vial2Bag Advanced® Admixture deviceVial → IV bag admixture Liquid or powder IV Bag IV bag port Needle‑free design; easy “cap-spike-admix" process; available in 13mm and 20mm format; universal* IV bag compatibility;


Regional Availability & Country‑Specific SKUs

Product availability can vary across different countries and regions. Certain configurations, sizes, sterilization methods, and interface options may be approved or distributed only within specific markets.

Because each region may have different SKU listings or regulatory statuses, customers should contact their local West representative for clarification and assistance in selecting the most appropriate device configuration.

West’s regional teams can provide:

  • Confirmation of available SKUs in your country
  • Guidance on region‑specific product approvals
  • Assistance with device selection for your workflow
  • Support for transitioning between product families

For accurate, region‑specific information, please contact West directly.

Want to Learn More?

Mix2Vial® and Mixject® are registered trademarks of West Pharma. Services IL, Ltd., a subsidiary of West Pharmaceutical Services, Inc.

Mix2Vial Transfer Device Indication, Safety and Warnings

The Mix2Vial® transfer device is 510(k) cleared by the United States Food and Drug Administration and carries the CE mark (0344). Products are shown for INFORMATION purposes only and may not be approved for marketing in specific regions. Distribution and use are subject to applicable regulatory approvals and requirements for medical devices. Failure to follow product instructions for use may result in loss of sterility; contamination; inadequate transfer, dilution, and/or withdrawal; and/or medication dosing. Product misuse could potentially lead to user and/or patient infection, suboptimal therapy, and/or delay in therapy. Please contact your West Pharmaceutical Services, Inc. (West) representative for product availability.