INDUSTRY COMPONENT

Plunger Rod

Precision plunger rod for medical-grade polypropylene syringes, ensuring accurate fluid delivery and patient safety.

Component Specifications

Definition
A critical cylindrical component within medical-grade polypropylene syringes, designed to create a sliding seal within the syringe barrel. It translates manual or automated force to displace medication or fluids with precise volumetric control. Its engineering ensures smooth operation, minimal friction, and compatibility with pharmaceutical formulations.
Working Principle
Operates on the principle of positive displacement. When force is applied to the thumb press, the plunger rod moves linearly within the syringe barrel. This movement creates pressure differentials, forcing the fluid through the needle or outlet. The seal (typically a rubber or elastomeric tip attached to the rod) prevents backflow and ensures accurate dosage delivery.
Materials
Medical-grade polypropylene (PP), complying with USP Class VI, ISO 10993, and FDA 21 CFR. May include additives for color coding (masterbatch) and enhanced rigidity. The tip seal material is typically bromobutyl or chlorobutyl rubber.
Technical Parameters
ParameterTypical rangeNotes & selection driver
Glide Force1-5 N
Length Range50-150 mm
SterilizationGamma radiation or Ethylene Oxide (EtO)
Surface FinishRa ≤ 0.8 μm
Breakloose Force3-10 N
Diameter Tolerance±0.05 mm

Ranges are indicative industry figures for RFQ preparation, not a supplier commitment. Confirm every value and standard with the legal manufacturer before ordering.

Standards
ISO 7886-1, ISO 11040-4, DIN EN ISO 13485

Parent Products

This component is used in the following industrial products

Engineering Analysis

Risks & Mitigation
  • Material leaching into medication
  • Sticking or jerky movement (stiction)
  • Seal failure causing leakage
  • Breakage under excessive force
  • Non-compliance with regulatory standards
FMEA Triads
Trigger: Inconsistent polymer molding leading to dimensional variation
Failure: Increased friction or leakage
Mitigation: Implement Statistical Process Control (SPC) on injection molding parameters and 100% automated dimensional inspection.
Trigger: Inadequate sterilization validation
Failure: Patient infection risk
Mitigation: Adhere to validated sterilization cycles (ISO 11135 for EtO, ISO 11137 for radiation) and perform routine biological indicator testing.

Industrial Ecosystem

Compatible With

Typical Suppliers & Equivalents

Compliance & Inspection

Tolerance
Geometric tolerances per ISO 2768-m, critical dimensions per customer drawing ±0.05mm
Test Method
Dimensional: CMM; Forces: tensile tester with custom fixture; Extractables: HPLC/GC-MS; Biocompatibility: ISO 10993 series

Procurement Evaluation Criteria

A practical evidence checklist for RFQ preparation and supplier evaluation.

Technical documentation
Request current drawings, revision history, and a signed specification sheet.
Manufacturing capability
Verify equipment lists, process limits, capacity, and representative production evidence.
Inspection readiness
Confirm test methods, calibrated equipment, sampling plans, and traceable reports.
Supplier transparency
Check the legal entity, factory address, ownership, certifications, and direct contacts.

CNFX does not score or rank suppliers. Buyers must verify all claims and documents with the legal manufacturer before ordering.

Manufacturers of Plunger Rod

Manufacturer profiles associated with Plunger Rod.

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Frequently Asked Questions

What are the critical quality tests for a plunger rod?

Key tests include dimensional verification, breakloose and glide force measurement, extractables/leachables analysis, biocompatibility testing (ISO 10993), and functionality under simulated use conditions.

Can plunger rods be interchanged between syringe brands?

No, plunger rods are typically designed for specific syringe barrel geometries and seal configurations. Interchangeability is limited unless explicitly validated by the manufacturer to ensure performance and safety.

Data Basis

Editorial classification, named public sources where available, and source-reviewed manufacturer records. See the editorial policy.

Preliminary Technical Classification
This page supports structured research, RFQ preparation, and supplier evaluation. It does not replace buyer-led supplier qualification, standards review, or technical approval.

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