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Home > Blog > Technology & Testing
EasyPumpVac Biocompatibility Testing Explained What the ISO 10993 Results Actually Support
March 17th, 2026

EasyPumpVac Biocompatibility Testing Explained What the ISO 10993 Results Actually Support

A technical analysis of the official biological-evaluation reports for EasyPumpVac FAC-01. This article explains what the cytotoxicity, intracutaneous irritation, and skin sensitization studies actually support about material-contact safety under the stated test conditions, and why that evidence matters for homes, schools, and other staged-use settings.
EasyPumpVac Accelerated Aging Test: What the FAC-01 Report Actually Shows
March 17th, 2026

EasyPumpVac Accelerated Aging Test: What the FAC-01 Report Actually Shows

A technical analysis of the official laboratory accelerated aging report for EasyPumpVac FAC-01. This article explains what the report actually documents, how the Q10 = 2 model and AAF = 11.3 were used to calculate 1-year and 2-year time-equivalent storage exposure, and why that matters in a storage-readiness discussion without overstating what the report proves.
Inside the Lab: What 19–42 kPa Means for EasyPumpVac and FoldPumpVac Updated on March 17, 2026
March 12th, 2026

Inside the Lab: What 19–42 kPa Means for EasyPumpVac and FoldPumpVac Updated on March 17, 2026

A technical overview of FITIGER's EasyPumpVac and FoldPumpVac negative-pressure testing program, including bench testing across different stroke lengths and conditions, volunteer observations, and why suction characterization matters for both obstruction removal and avoidance of unnecessary soft-tissue loading.
Biological Safety Testing for FoldPumpVac: What FITIGER's ISO 10993/GB/T 16886 Results Mean for Parents Updated on March 17, 2026
March 11th, 2026

Biological Safety Testing for FoldPumpVac: What FITIGER's ISO 10993/GB/T 16886 Results Mean for Parents Updated on March 17, 2026

A technical review of FoldPumpVac patient-contact biological safety testing, written from Fitiger’s engineering and product safety team perspective. This article explains what our cytotoxicity, irritation, and sensitization results mean, how those tests fit within the ISO 10993 framework, and how parents should interpret laboratory data responsibly.
FoldPumpVac Cleaning and Disinfection Validation: What Our Reprocessing Reports Mean for Airway Readiness Updated on March 17, 2026
March 5th, 2026

FoldPumpVac Cleaning and Disinfection Validation: What Our Reprocessing Reports Mean for Airway Readiness Updated on March 17, 2026

A technical analysis of FoldPumpVac FAC-02 reprocessing validation. This article explains why protein clearance matters before disinfection, how the validated 75% ethanol method performed against multiple test organisms including Mycobacterium terrae, and what these reports support for hygiene readiness in schools, homes, and other preparedness settings.
EasyPumpVac Disinfection Validation Technical White Paper
March 5th, 2026

EasyPumpVac Disinfection Validation Technical White Paper

Based on third‑party laboratory reports (CY2506164N‑4 / CY2506164N‑3), this white paper explains why Fitiger EasyPumpVac (FAC‑01 platform) requires validated reprocessing (cleaning + disinfection) and summarizes worst‑case challenge results
Fitiger Anti-Choking Device Technical Performance White Paper (Summary) I
February 24th, 2026

Fitiger Anti-Choking Device Technical Performance White Paper (Summary) I

It summarizes third-party accelerated aging parameters for EasyPumpVac and FoldPumpVac, translating key conditions (Q10, temperatures, AAF, time equivalents) from Fitiger inspection reports to support documentation and storage readiness. Built for emergency preparedness, this brief explains why aging control matters for a choking rescue device f
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