Standard pump-set configurations
Established fluid-path configurations for review against a specified pump model and operating conditions.
Choose an existing configuration for a specified pump, or develop a dedicated set around your own pump platform.
Use these routes to identify the closest BQ+ configuration concept. The exact REF, pump interface, operating conditions and destination-market requirements are confirmed before release.
Established fluid-path configurations for review against a specified pump model and operating conditions.
Configurations reviewed against the specified pump segment, tubing interface and intended operating range.
Selected chamber and fluid-stop concepts, subject to product-specific functional and market review.
Choose the closest structure, then send the pump model and any required changes. Current availability and released specifications are confirmed by BQ+ product reference.
Vented drip chamber, pump segment, roller clamp and male luer connection.
Pump clamp, roller clamp, slide clamp and one injection access point.
Two needle-free access points with a check valve and standard flow-control components.
In-line liquid filter with an access point, clamps and male luer connection.
In-line precision filter with a needle-free access point and standard clamps.
Check valve, in-line filter and two needle-free access points in an extended fluid path.
Three needle-free access points with a check valve and standard flow-control components.
Silicone pump segment with selectable upstream and downstream tubing and connections.
The pump segment is one part of the product. Around it, BQ+ offers a broad selection of standard infusion-set components for the complete fluid path.
A BQ+ pump-segment platform for projects where PVC tubing is selected. Material, dimensions, pump fit and applicable performance claims are confirmed for the specified product and evidence package.
Silicone pump segments can be configured with the required upstream and downstream connections and the selected standard fluid-path components.
Anti-free-flow mechanisms, stop-flow clamps, pump-loading clips, holders, cassettes and other pump-interface parts are generally specific to the pump manufacturer’s design. BQ+ can support tooling development and controlled manufacturing based on approved design inputs. Customer-specific drawings, dimensions and component details are not publicly disclosed.
The pump segment is selected for the specified pump. The remaining fluid path can then use the same broad BQ+ component platform shown below.
Each category shows four representative choices where the catalog contains more than four options, with the wider range linked to the exact catalog pages.
These are shared component-selection references. Pump tubing, loading parts, anti-free-flow mechanisms and other pump-specific interfaces remain configuration- and project-specific.
The final arrangement depends on the intended application, workflow and evidence requirements. Each function is evaluated for the defined project.
Container interface, drip chamber, tubing, clamps, access points and patient-end connection around the target pump.
Selected filtration or light-protection functions evaluated with the finished fluid path and defined test conditions.
Project-specific review of filtration, materials, operating conditions, pump interface and market pathway.
Dedicated nutrition-delivery configurations separated from I.V. products with appropriate connectors and risk controls.
Branches, access points, connectors, check valves and other functions considered within the defined fluid path.
A market reference or current set can start comparison. Equivalence is not assumed from appearance or catalog number alone.
Each stage answers a different question and creates a clearer handoff between the customer team and BQ+.
Define the pump, application, market, reference product, fluid path, packaging and open questions.
Compare the request with documented component and set platforms and identify the development gap.
Separate layout, pump-fit, functional, pilot-process and validation samples by purpose.
Agree the tests and records needed for the selected pump, configuration, intended use and market.
Align drawings, BOM, specifications, manufacturing controls, packaging and change responsibilities.
Once we know the configuration you need, BQ+ reviews the complete fluid path before preparing a quotation, sample or technical file.
BQ+ can coordinate component selection, tubing, interfaces, finished-set assembly, packaging and sterilization planning within one development workflow.
The exact manufacturing scope is confirmed for each project. “Coordinated” does not mean every process is automatically in-house.
BQ+ can evaluate a dedicated set around a customer-specified pump. Final compatibility is limited to the defined pump model and validated set configuration.
No. A pump, current set, dimensional specification, sketch or marked-up sample can begin the review.
Not automatically. Layout and pump-fit samples may support concept or interface review but may not represent the intended production process.
Timing depends on requirement maturity, platform fit, tooling or material changes, sample stages, evidence, packaging, sterilization and market pathway. A project plan follows the initial review.
By product reference, configuration, intended use, manufacturing site, destination market and current record. One clearance or certificate is not automatically extended to a new pump-specific set.