eBAG 3D STR for single use bioreactor solution

A TECNIC single-use bag with the name eBAG® 3D STR, it is transparent and rectangular but with rounded edges.

transparent cylindrical and bioprocess bag (eBAG® 3D STR) with rounded edges (supplies) for bioprocessing equipment

Dedicated to overcoming the limitations of single-use bag systems

Advanced eBAG 3D STR for dual-purpose single fermenter/bioreactors

In the ever-evolving landscape of Biotech, TECNIC's Single-Use eBAG 3D STR is ingeniously designed to seamlessly integrate with our dual-purpose Single-Use bioreactor. Devoted to overcoming the inherent limitations in single-use systems, the eBAG 3D STR stands as a purpose-built, cutting-edge solution tailored for mammalian culture. As well as, this innovative system is meticulously crafted to tackle specific challenges, offering a transformative leap in the capabilities of microbial bioprocessing.

Produced under stringent aseptic conditions and subjected to comprehensive sterilization, these bags ensure high sterility and minimal contamination risk. With customizable features catering to specific size configurations and fittings, they seamlessly integrate into manufacturing processes.

Developed and Manufactured in TECNIC ISO7 Clean Room, eBAG 3D STR is built tough with high-quality materials and undergo gamma irradiation. As a result, they are ready-to-use according to the strictest pharmaceutical industry standards and are available in various sizes (30L up to 1000L). They can withstand rigorous handling to ensure the safe containment of biopharmaceutical products. Perfectly designed to work with TECNIC ePILOT and ePROD Single Use Bioreactor ⇀, manufactured to perfectly fit into the tank and fully adapt with the fully magnetic mixer to provide assurance in your process.

Guaranteed sterility for sensitive bioprocesses

Sterility assurance

Modular system

Cost-effectiveness

Various configuration options

Bag scalability

Quality assurance

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Film technology for enhanced bioprocess

Our TECNIC Film Technology is specifically engineered for high-quality. Every one of our Single-Use products distinguishes itself by its unique five-layer structure, with each layer serving a specific function to optimize the integrity, durability, longevity and the sterility of the equipment.

Layer 1 - LPDE (50μm)

The first layer is made of Low-Density Polyethylene (LPDE) provides the Single-Use products with a robust mechanical strength, ensuring durability and resistance to physical factors. Is the outer shell that protects the bag from external factors and handling damages.

Layer 2 - TIE (10μm)

Layer 3 - EVOH (20μm)

Layer 4 - TIE (10μm)

Layer 5 - ULPDE (230μm)

In-house ISO 7 cleanroom for single-use standards

The manufacturing process for our single-use bioprocessing products, such as the eBAG® 2D, 3D and SU vessel, strictly complies with the rigorous standards of an ISO 7 cleanroom This specific classification guarantees a highly controlled environment, characterized by a maximum particle count of 10,000 (≥ 0.5 μm) per cubic meter of air.

This level of control is critical for ensuring the sterility and quality of our products, as it significantly reduces the risk of microbial and particulate contamination. By adhering to these standards, we ensure that each product meets the high expectations of purity and performance required in sensitive bioprocessing applications, providing our clients with reliable and consistent biotechnological solutions.

Two people covered entirely in white clothing working in a clean room in a scientific application.

through a window, people can be seen in a single-use plant working

High standards in bioprocessing

The eBAG represents not just an innovation in cell culture film technology, but also sets new benchmarks in quality and regulatory compliance. Each eBAG is manufactured under stringent Good Manufacturing Practices (GMP), ensuring that every product meets the highest standards of quality and safety.

Sterilization is a critical aspect of production. We employ advanced radiation sterilization methods, effectively eliminating biological contaminants without compromising the product's integrity. This sterilization process is crucial for maintaining sterility and safety in sensitive applications.

Furthermore, the production of eBAG takes place in inhouse ISO 7 classified facilities. These cleanrooms are designed to control contamination and maintain an aseptic environment, essential for the manufacturing of biotechnological products. Adhering to ISO 7 standards ensures that each eBAG is produced in a controlled environment, minimizing the risk of cross-contamination and ensuring product consistency.

Together, these quality measures and regulatory compliance reflect our commitment to excellence in manufacturing eBAG®, providing our clients with reliable and safe products for their critical bioprocessing applications.

Test	Requirements	Results
USP <788> Particulate Matter in Injections	Pass	Pass
USP <88> Systemic Toxicity	Pass	Pass
USP <88> Intracutaneous	Pass	Pass
USP <88> Implantation	Pass	Pass
USP <87> Cytotoxicity, Agar Diffusion	Pass	Pass
USP <87> Cytotoxicity, Elution	Pass	Pass
USP <85> Kinetic-Chromogenic LAL	0,25 EU/ml	0,006 EU/ml
USP <661.1> Physicochemical-Non Volatile	15 mg	1 mg
USP <661.1> Physicochemical-Residue on Ignition	5 mg	1 mg
USP <661.1>Physicochemical-Heavy Metals	1 ppm	1 ppm
USP ≤661.1>Physicochemical-Buffering Capacity	10 ml	1 ml
ISO 10993-4 In-Vitro Hemolysis Study	Non-haemolytic	Non-haemolytic
Irradiation Dosage	25-50 kGy	25-50 kGy
EP <3.2.2.1> Plastic Containers for Aqueous Solutions for Parenteral Infusion	Pass	Pass

The eBAG® represents not just an innovation in cell culture film technology, but also sets new benchmarks in quality and regulatory compliance. Each eBAG® is manufactured under stringent Good Manufacturing Practices (GMP), ensuring that every product meets the highest standards of quality and safety.

Furthermore, the production of eBAG® takes place in inhouse ISO 7 classified facilities. These cleanrooms are designed to control contamination and maintain an aseptic environment, essential for the manufacturing of biotechnological products. Adhering to ISO 7 standards ensures that each eBAG® is produced in a controlled environment, minimizing the risk of cross-contamination and ensuring product consistency.

Test	Requirements	Results
USP <788> Particulate Matter in Injections	Pass	Pass
USP <88> Systemic Toxicity	Pass	Pass
USP <88> Intracutaneous	Pass	Pass
USP <88> Implantation	Pass	Pass
USP <87> Cytotoxicity, Agar Diffusion	Pass	Pass
USP <87> Cytotoxicity, Elution	Pass	Pass
USP <85> Kinetic-Chromogenic LAL	0,25 EU/ml	0,006 EU/ml
USP <661.1> Physicochemical-Non Volatile	15 mg	1 mg
USP <661.1> Physicochemical-Residue on Ignition	5 mg	1 mg
USP <661.1>Physicochemical-Heavy Metals	1 ppm	1 ppm
USP ≤661.1>Physicochemical-Buffering Capacity	10 ml	1 ml
ISO 10993-4 In-Vitro Hemolysis Study	Non-haemolytic	Non-haemolytic
Irradiation Dosage	25-50 kGy	25-50 kGy
EP <3.2.2.1> Plastic Containers for Aqueous Solutions for Parenteral Infusion	Pass	Pass

Test	Need	Result
USP <788> Particulate Matter in Injections	Pass	Pass
USP <88> Systemic Toxicity	Pass	Pass
USP <88> Intracutaneous	Pass	Pass
USP <88> Implantation	Pass	Pass
USP <87> Cytotoxicity, Agar Diffusion	Pass	Pass
USP <87> Cytotoxicity, Elution	Pass	Pass
USP <85> Kinetic-Chromogenic LAL	0,25 EU/ml	0,006 EU/ml
USP <661.1> Physicochemical-Non Volatile	15 mg	1 mg
USP <661.1> Physicochemical-Residue on Ignition	5 mg	1 mg
USP <661.1>Physicochemical-Heavy Metals	1 ppm	1 ppm
USP ≤661.1>Physicochemical-Buffering Capacity	10 ml	1 ml
ISO 10993-4 In-Vitro Hemolysis Study	Non-haemolytic	Non-haemolytic
Irradiation Dosage	25-50 kGy	25-50 kGy
EP <3.2.2.1> Plastic Containers for Aqueous Solutions for Parenteral Infusion	Pass	Pass

Bag properties

Robust exterior layer

All of TECNIC Single-Use products are designed with a robust construction to guaranteeing the secure containment of the product. The mechanical strength of our products ensures durability and resistance to external physical factors.

Sterile environment

Temperature resilience

GMP and ISO standards

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