Manufacturing Platform
ALSPL manufactures medical devices across interventional, critical care, renal and surgical categories with integrated in-house production capability
Manufacturing is structured around dimensional tolerance control, validated bonding processes and repeatable production parameters to ensure clinical reliability
Core Manufacturing Areas
Balloon Technology
Balloon forming, neck shaping, and balloon-to-shaft integration.
Catheter Systems
Complete balloon catheter assembly, shaft integration, and validation.
Guidewire Platforms
TAVI wires and micro-diameter hybrid neuro wires down to 0.007".
Injection Moulding & Integration
High-precision production of dilators, hubs, connectors, torque devices and structural housings with multi-component integration
Sterile Assembly
Procedure kit configuration and sterile assembly integration.
OEM Partnerships
ALSPL supports medical device companies with disciplined production and scalable platform solutions.
Established Designs
Commercial production of existing device designs.
Site Transfers
Transfer of manufacturing from alternate facilities.
Private Label
Production under defined drawings & specs.
Consolidation
Multi-product programs under one platform.
Program Deliverables
- Component-only supply
- Sub-assembly manufacturing
- Finished sterile devices
- Balloon catheter systems
- Advanced Guidewire systems
- Full procedure kit assembly
Production is aligned to documented specifications, controlled tooling and validated performance verification
Tooling & Process Control
Manufacturing programs are supported by rigorous validation and performance verification protocols.
Moulding & Tooling
- Tool design & cavity validation
- Controlled polymer moulding
Catheter & Balloon
- Shaft integration & bonding
- Forming & burst pressure testing
Guidewire Engineering
- Stiffness tuning & tip alignment
- Mechanical performance verification
Assembly Control
- Multi-component configuration
- Structured process documentation
Quality & Regulatory Alignment
Manufacturing operates within structured quality systems aligned to regulated medical device markets.
- Lot Traceability
- Process Documentation
- Production Controls
Supporting domestic and international supply programs with full compliance.