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Production of body compatible surgical materials

The production of biocompatible surgical materials encompasses the development and production of biocompatible instruments, implants, and sutures used during surgical procedures. Current challenges in this field include strict compliance with regulatory requirements and ensuring the highest quality standards. Trends such as the use of advanced materials, including biocompatible polycarbonates and titanium alloys, and the integration of Industry 4.0 technologies for process optimization are shaping the industry. These developments aim to increase patient safety and improve efficiency in surgical practice.

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ACJ 200-4M
ACJ 200-4M

Analysis of the shrinkage behavior of a fabric sample. The change in a substance when it comes into contact with water or steam is decisive for further processing. Knowing about the properties of a material allows a better and more precise use of this material

FK 10
FK 10

A folded vascular prosthesis is tested for its behavior during expansion and contraction to reliably assess its extension behavior. This allows for a targeted evaluation of the prosthesis's functional suitability and ensures the quality of its fabrication.

HDD 100-1
HDD 100-1

Epoxy resin coatings for internal sensors are tested for complete curing to reliably ensure the product's safe functionality. This allows for the early detection of insufficiently cured components and the avoidance of potential risks to the patient.

DS 20K0.1
DS 20K0.1

The individual components for a suspension solution are precisely weighed to reliably ensure the required composition for further processing. This prevents deviations in the process and supports consistent quality in the subsequent application.

EW 2200-2NM
EW 2200-2NM

During the dilution process, color solutions are precisely weighed in 10 mg increments to ensure the desired dilution is achieved exactly. This allows for stepwise dosage control and guarantees a reproducible, error-free result.

PNJ 3000-2M
PNJ 3000-2M

The particle size of powders is determined in a sieving process by precisely weighing the individual fractions to reliably verify defined limits. This allows deviations to be detected early and prevents defective production batches.

TVO 2000N500S
TVO 2000N500S

Vascular prostheses made of plastic or textile materials undergo a tensile test to reliably assess their tear resistance and ensure they meet the required load-bearing capacity. This allows defective specimens to be identified early and selectively sorted out before further processing.

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