Pharmaceutical Industry

Precision Components for Safer, Smarter Medical Devices

Solution

Pharmaceutical & Lab Precision Systems

Pharmaceutical Primary Packaging

Pharmaceutical Primary Packaging

Vials & Ampoules: USP compliant Type I borosilicate glass, available in sterile/lyophilized formats.
Pre-Filled Syringes: ISO certified, with silicone oil-free options for biologics.
Custom Closures: Flip-off seals, elastomeric stoppers (ISO validated).

Medical Kit Components

Medical Kit Components

Sterile Pouches & Blister Packs: ISO compliant, with ethylene oxide (EO) or gamma sterilization.
Diagnostic Device Parts: PCR tube racks, microplate holders (CNC-machined, ±0.02mm tolerance).

Lab Consumables

Lab Consumables

High-Precision Pipette Tips: DNase/RNase-free, validated per ISO.
Cryogenic Vials: Compatible with liquid nitrogen storage (-196°C), USP Class VI materials.

Solution

Our Service

Understanding Your Needs

Understanding Your Needs

Precision Starts with Your Requirements

Regulatory-First Approach: Dedicated team navigates country-specific compliance (e.g., FDA 510(k), CE Marking, MDR).

Needs Analysis Workshop: Joint sessions to align technical specs, budget, and certification timelines.

Free Regulatory Consultation: Pre-audit support for your local market entry requirements.

IP Protection Guarantee: NDAs and secure data protocols (GDPR compliant).

custom injection molding

Prototyping & Sampling

From CAD to Certified Samples in 72 Hours

Rapid Prototyping: CNC machining/3D printing for syringe components (tolerance ±0.01mm).

Pre-Shipment Testing: Samples validated against ISO 7864/ISO 9626 standards.

Free Global Courier: DHL/FedEx prepaid return service for sample approvals.

DFM Optimization: Reduce production costs by 15% through design enhancements.

Production & Inventory

Production & Inventory

Smart Manufacturing, Assured Quality

Zero-Defect Pledge: 7-stage QA process including vision inspection and leak testing.

Flexible MOQs: Start from 5,000 units with 30% safety stock for urgent orders.

Real-Time Monitoring: IoT-enabled production tracking via client portal.

Green Manufacturing: Energy-saving injection molding systems (30% lower carbon footprint).

Shipping & Logistics

Shipping & Logistics

Door-to-Door Medical Logistics Mastery

Global Network: Serve 50+ countries with DDP (Delivered Duty Paid) terms.

Cold Chain Solutions: Temperature-controlled shipping for sensitive devices.

Documentation Hub: Automated export docs (COO, SDS, commercial invoice).

98.7% On-Time Delivery: Real-time GPS tracking + customs pre-clearance.

After-Sales Support

After-Sales Support

Lifelong Partnership, Beyond Delivery

24/7 Multilingual Support: Engineers fluent in EN/ES/FR/AR.
Extended Warranty: 3-year product liability coverage.
RCA (Root Cause Analysis): Issue resolution within 48 hours.

Becoming a global leader in medical puncture devices

We are committed to pursuing technological innovation and continuous improvement to build the KDL brand, which is recognized and trusted by users around the world.
We believe that through our extraordinary efforts and insights, our products can make the lives of millions of users healthier and better through better treatment and care.
This is the vision of KDL and the common pursuit of each and every one of us.

ISO

End-to-End Manufacturing Expertise:

– Full industrial chain from raw material welding to precision
needle processing (ISO 13485 & FDA-compliant).

260+

Certified Excellence:

– 260+ global patents, CMDC/EU TUV/FDA certifications, and 106+ product registrations worldwide.

30+

Scalable Capacity:

– 30+ years of OEM/ODM experience with fully automated
production lines.

35%

Cost Efficiency:

– Optimized supply chain reduces lead times by 35% vs industry
benchmarks.

100%

Sustainability Commitment:

– ESG-aligned processes with 100% recyclable packaging.

No.

1

Leader in puncture medical devices,20% market share in China

106

+
registration certificates worldwide

260

+
patents worldwide

50

+
countries sales network
Laboratory Services

Advanced In-House Laboratory Services

Expert-Led Testing Teams

– PhD researchers with 15+ years in medical device analytics.
– Cross-functional collaboration with R&D for failure mode analysis (FMEA).

Global Compliance Support

Pre-submission testing packages for:
– EU MDR Annex XV Technical Documentation
– FDA 510(k) Substantial Equivalence
– WHO Prequalification (PQ) dossiers

Explore Your Sourcing Solution

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