Pharmaceutical Testing Instrument Manufacturer & Supplier
MedIntegrity is the manufacturer and U.S. supplier of every instrument on this page — each line designed and built in our own factory, 28 patented products across the portfolio.
All Product Lines
Seven product lines, 19 instrument models — the complete set for integrity testing in pharmaceutical manufacturing: filter integrity, glove integrity, container-closure integrity, packaging leak detection, RTP integrity, TOC analysis and freezing-point osmolality.
Filter Integrity Tester
Sterilizing-grade liquid filter integrity testing — bubble point, diffusive flow, pressure hold and vacuum decay methods for pre-use, post-use and PUPSIT verification.
IntegtestV6.5 / IntegtestV8.0 →
Bubble Point Tester
Bubble point testing for membrane filters — fast, non-destructive verification of sterilizing-grade filtration per USP <43> and EP 11.0.
IntegtestV6.5 / IntegtestV8.0 →
Glove Integrity Tester
Wireless pressure-decay glove integrity testing for isolators, RABS and glove boxes — detect leaks down to 100 µm, electronic records for ≥5 years.
WGT-1000 / WGT-1200 →
Container Closure Integrity (CCI)
CCIT systems for vials, prefilled syringes and sterile drug packaging — deterministic pressure-decay testing per USP <1207>.
system overview →
Packaging Leak Tester
Seal and leak integrity testing for pharma packaging — blister, pouch, sachet and rigid containers with traceable electronic records.
MFT-600 / MFT-800 / MFT-900 / MFT-1000 →
RTP Integrity Tester
RTP integrity testing instruments for aseptic pharma production lines, with electronic records and IQ/OQ/PQ documentation.
WRTP-1000 / WRTP-1200 →
Bag Integrity Tester
Leak detection for fluid bags and pouches — pressure-decay method with electronic records for pharmaceutical bag manufacturing and QC.
BGT-5000 / BGT-120 / BGT-200 →
Total Organic Carbon (TOC) Analyzer
TOC analysis for pharmaceutical water systems and process water — laboratory and semi-online analyzers with automated sampling options.
TA-2.0 / TA-3.0 / TA-100 / TA-200 / AIS-2.0 →
Freezing Point Osmometer
Freezing-point-depression osmolality testing for injectables, biologics and reference standards — precise, sample-sparing measurement.
FPOSM-V3.0 →How to Find Your Instrument
Each model has its own specification page with the full parameter table, method background and qualification documentation scope. The category pages give the overview — the method set, the standards context and the model selection guidance — and link through to every model in the line.
Start from the application: what has to be verified, on what, and at which stage — fill, in-process, release, or routine qualification. That usually pins down the product line, and the model selection inside it comes from the container format, test volume and the acceptance limits your program defines.
Not sure where you sit in the matrix? Send us the application and the pharmacopeia requirements, and we will come back with the instrument, the method set and the acceptance criteria — before you commit to anything.
Need a quote or technical advice?
Tell us your application — our U.S. team responds with product selection, documentation and pricing.
Request a Quote