CryoLoc™ CV

Cardiovascular Freezing Bags and Overwraps

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CryoLoc™ CV

Store cardiovascular tissues during cryopreservation, storage, transport, and aseptic presentation.

The CryoLoc™ CV Line is specifically engineered to provide complete protection for cardiovascular (CV) tissues during cryopreservation, storage, and transport. With its innovative design and highly inert materials and with customizable pouch systems, built-in traceability, and aseptic presentation in the OR, CryoLoc CV is the ideal solution for cardiovascular tissue preservation.

Dual-Pouch System

The CV line consists of a primary (inner) pouch, designed with a rounded structure to cradle CV tissues securely. The inner pouch fits perfectly within an outer peel pouch, providing full protection and ease of handling. The dual-pouch system also allows for the aseptic presentation of tissues within the operating room.

-190°C Protection

Built to withstand extreme cryogenic temperatures, ensuring that tissues are fully protected throughout the entire process.

Highly Inert Materials

Designed to be highly inert to cryopreservation agents, including DMSO, maintaining the integrity of the tissues.

USP Class VI Compliant

Manufactured from materials that conform to USP Class VI standards, ensuring the highest level of safety and biocompatibility.

Traceability with Lot Numbers

CryoLoc™ bags are lot number tracked for easy traceability, ensuring full compliance wih regulatory requirements.

Multiple Configurations

Available in two versions – CV and aortoiliac – both offered in either a two-pouch or three-pouch system for customizeable protection.

Label Pocket Options

CryoLoc™ Overwrap includes integrated label pockets for traceability and compliance.

Standard CV Kit

Standard CV Kit

Triple CV Kit

Triple CV Kit

Applications

Cryopreservation of cardiovascular tissues for transplantation
Long-term storage of cardiovascular and aortic iliac tissues
Safe transport and aseptic presentation of cryopreserved cardiovascular tissues within the operating room

Cleanroom-to-Cleanroom™
Delivery Model

Our Cleanroom-to-Cleanroom™ model ensures that Instant Systems’ products remain in a sterile environment from production to delivery. Manufactured and packaged within our Class 6 Cleanroom, each product is encapsulated in specialized packaging that maintains this pristine environment so that when you open it in your cleanroom, the product is as clean and safe as when it left our facility.

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    Distribution

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    Methods which integrate with your systems, delivering product to you or your customers’ locations securely and on time.
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    Procurement

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    Our experts create a highly flexible procurement service, tailored to your needs to increase efficiencies and reduce costs.
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    • - Fully redundant manufacturing facilities
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    Supply Chain Management

    BOUNDLESS OPPORTUNITIES
    Instant Systems Supply Chain Management services offers the operational and financial foundation to provide extraordinary protections and endless opportunities for growth for the clients we serve.
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    • - Fully redundant manufacturing facilities
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    Testing & Validation

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    Full service validation, including protocol writing, testing specification documentation, test execution, project management, and final reporting, allows you to leverage our team’s expertise to achieve your objectives quickly.
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    STERILIZATION

    EO, STEAM, GAMMA
    Choosing the best sterilization method must take into consideration many factors such as design, materials, packaging, and final case configuration. Because no sterilization method is right for every applications.
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    • ISO 9001/13485 Documented Procedures
    • 21 CFR 820 Compliant Quality Management System
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    • - Fully redundant manufacturing facilities
    • - Cross-validated equipment
    • - Cross-trained technicians
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    Kitting & Assembly

    Quality no matter the quantity
    Our highly skilled technicians assemble and kit to your requirements with meticulous accuracy. All assemblies are controlled and verified through Instant Systems’ Quality Management System to provide complete traceability.
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    • ISO 9001/13485 Documented Procedures
    • 21 CFR 820 Compliant Quality Management System
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    • - Fully redundant manufacturing facilities
    • - Cross-validated equipment
    • - Cross-trained technicians
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