IMI


Manufacturer and developer of single-use drug-delivery components and tamper-evident closure systems for hospitals, pharmacies and compounding facilities. Offers design, large-scale injection molding, cleanroom assembly and automated packaging of medical-grade plastic devices, with regulatory certifications (FDA registration, ISO 13485, MDSAP) and a focus on preventing drug diversion through tamper-evident technology.

Industries

Health Care
Manufacturing
Medical Device
Medical Equipment Manufacturing

Nr. of Employees

medium (51-250)

IMI

Pompano Beach, Florida, United States


Products

Tamper-evident caps for IV syringes

Closure devices for IV syringes that provide visible indication of tampering to support medication integrity and diversion prevention.

Luer lock caps and plugs

Luer lock and luer slip caps and plugs for capping and intermittent closure of syringes and ports.

Fluid-transfer connectors and guarded luer adapters

Connectors and adapters that facilitate safe transfer of fluids between syringes and infusion sets, including guarded/secured variants.

Medical aspirating and venting needles

Stainless-steel fill/aspirating needles and filtered venting needles suitable for fill/extraction and venting of hazardous compounds.

Tamper-evident caps with RFID

Closure components that include embedded RFID for device-level tracking and inventory/anti-diversion workflows.

Prep-Lock

IMI’s Tamper Evident Cap with Male Luer Lock delivers a secure closure solution that supports streamlined workflows and protects medication integrity from pharmacy to patient. Engineered for use with CADD medication cassettes, this cap offers a standardized approach to tamper-evident security, helping healthcare providers prevent drug diversion.

View All Products

Services

Design, prototyping and high-volume production of single-use drug-delivery components and closures using injection molding and cleanroom assembly.

Provision of complimentary sample units for product evaluation by prospective customers.

Support related to regulatory certifications and quality management practices aligned with ISO 13485 and MDSAP frameworks.

Expertise Areas

  • Tamper-evident device design for drug security
  • Medical device manufacturing and injection molding
  • Regulatory compliance and quality management (FDA, ISO 13485, MDSAP)
  • Supply chain and distributor channel management
  • Show More (2)

Key Technologies

  • Tamper-evident closure systems
  • Injection molding of medical-grade plastics
  • Cleanroom assembly and automated packaging
  • Radio-frequency identification (RFID)
  • Show More (2)

News & Updates

Announcement of successful completion of a Quality Management System audit under the Medical Device Single Audit Program (MDSAP).

Announcement of closure components released with embedded RFID for tracking and anti-diversion use cases.

Participation in an industry consortium focused on RFID technology in healthcare.

Availability announcement for a tamper-evident cap designed for use with CADD medication cassettes.

Three-part blog series providing guidance on aseptic processes and internal mock inspections for sterile compounding.

Case example of implementing tamper-evident caps for pediatric syringe systems at a children’s hospital.

View All News

Similar organizations

Browse all ORGANIZATIONS

JOIN OUR MAILING LIST

Stay Connected with MTEC

Keep up with active and upcoming solicitations, MTEC news and other valuable information.