Infusion & fluid-path product platforms

Find the right product route before defining the details.

BQ+ supports established product families, configurable platforms and controlled co-development. Start with the clinical workflow or closest product family, then confirm the exact configuration, evidence and market pathway by BQ+ product reference.

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Representative BQ Plus infusion administration set
Representative BQ+ product configuration
Start with the workflowGravity, pump, transfusion, enteral or specialty
Find the closest familyUse existing products before custom development
Configure controlled optionsReview components as one system
Release by BQ+ REFKeep evidence and status traceable
Product portfolio

A broad platform—organised so buyers can find the right route.

Each family opens a different selection or development path. Exact options and claims remain configuration-specific.

Representative BQ Plus Gravity Infusion Sets configuration01

Gravity Infusion Sets

Standard, filtered, flow-regulated, needle-free, multi-access, burette and light-protected routes.

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Representative BQ Plus Pump Administration Sets configuration02

Pump Administration Sets

Existing compatible configurations and pump-manufacturer co-development around a specified pump.

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Representative BQ Plus Extension Sets & Multi-line Assemblies configuration03

Extension Sets & Multi-line Assemblies

Standard-bore, microbore, valve, filter, specialty and defined-pressure routes.

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Representative BQ Plus Blood Transfusion Sets configuration04

Blood Transfusion Sets

Gravity and defined-pump routes with controlled chamber and filter selection.

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Representative BQ Plus Enteral Feeding & Nutrition configuration05

Enteral Feeding & Nutrition

Feeding bags, spike sets, administration sets, extensions, syringes and pump projects.

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Representative BQ Plus Fluid-path Components configuration06

Fluid-path Components

A function-led component platform for finished-set development and defined supply.

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Representative BQ Plus Oncology Infusion Pathways configuration07

Oncology Infusion Pathways

Primary, secondary, pump and extension configurations for defined projects.

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Representative BQ Plus TIVA Infusion Sets configuration08

TIVA Infusion Sets

Finished two-line and three-line configurations selected by line function, pump source and exact product reference.

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Representative BQ Plus U.S. Catalog Onboarding configuration09

U.S. Catalog Onboarding

Compare a market reference with a controlled BQ+ configuration and exact regulatory path.

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Representative BQ Plus Infusion Accessories configuration10

Infusion Accessories

A model-led catalog of connectors, valves, clamps, filters and specialty fluid-path accessories.

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Representative BQ Plus Veterinary Infusion Sets configuration11

Veterinary Infusion Sets

Finished gravity, pump and extension configurations for defined veterinary applications.

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Representative BQ Plus Interventional and Pressure Monitoring Fluid Sets configuration12

Interventional & Pressure Monitoring Fluid Sets

Angiographic and pressure-monitoring fluid paths organised by procedure route and line configuration.

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Build the controlled configuration

Compare the complete pathway, not one isolated feature.

01Choose the product family
02Map the complete fluid path
03Confirm the controlled BQ+ REF
04Review evidence and market status
1
Clinical workflowDefine where and how the product is used
2
Product familySelect the closest established BQ+ route
3
Fluid-path configurationMap every interface, tube, valve, filter and control
4
Evidence routeIdentify tests and documents for the exact configuration
5
Market pathwayConfirm site, label, registration and release responsibilities
Configuration-specific evidence

Evidence belongs to the selected product.

These are review areas, not family-wide performance claims.

  • Controlled drawing and bill of materials
  • Materials and connection evidence
  • Functional verification by configuration
  • Packaging and sterilization
  • Label and IFU
  • Destination-market documentation
Release boundary: public values and regulatory wording require the exact BQ+ REF, current controlled evidence and specialist approval.
Start with what you know

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A drawing is helpful but not required. A sample, catalog reference or marked-up photograph can begin the review.

Send your requirement
  • Product family or workflow
  • Target country or region
  • Reference, drawing or sample
  • Required configuration
  • Packaging and private label
  • Technical documents required
  • Expected demand
  • Target timing
FAQ

Questions buyers ask before requesting a configuration.

Does BQ+ offer standard products or only custom development?

Both. The fastest route is usually to identify the closest controlled product family first.

Can a competitor catalog number start the review?

Yes. It is a comparison input, not proof of equivalence.

Do all products share one regulatory status?

No. Status is confirmed by exact BQ+ product reference, configuration, site, market and current record.

Can BQ+ develop around a customer pump?

Selected pump projects can follow a controlled co-development and verification route.