Certifications & Testing Reports
ISO 13485:2016 Quality Management System
CREDITECH MED operates under an ISO 13485:2016 quality management system, applying internationally recognized medical device manufacturing principles to the production of tattoo cartridge needles, PMU cartridges, and SMP solutions.
The quality system establishes standardized procedures for production control, documentation management, risk control, inspection processes, and continuous improvement to ensure consistent product quality and reliability.
EO Sterilization Compliance
TÜV SÜD ISO13485 ETO Sterilization Certification
To ensure product safety and sterilization reliability, CREDITECH MED works with qualified sterilization service providers operating under internationally recognized quality management standards.
Material Verification & Control
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FDA Compliance Testing Report
CREDITECH MED conducts material safety testing for cartridge components according to applicable FDA requirements to verify material safety and chemical stability.
The polypropylene (PP) material used in cartridge components has been tested for total extractable substances to support product safety and reliability.
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CE Compliance Verification
CREDITECH MED tattoo cartridge needles undergo compliance verification to ensure conformity with applicable European safety and environmental requirements.
The verification covers product testing according to relevant EU directives, supporting reliable product quality and compliance for global markets.
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Membrane Material Test Report
The membrane is a critical component inside tattoo cartridge needles, providing reliable sealing and helping prevent ink and fluid backflow during operation.
CREDITECH MED verifies membrane material properties through testing reports to ensure consistent quality, durability, and reliable performance for professional tattoo cartridge applications.
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Housing Material MSDS Report
The cartridge housing is an essential structural component of tattoo cartridge needles, providing protection, stability, and reliable support for internal components.
CREDITECH MED provides material safety documentation (MSDS/SDS) for housing materials to verify material composition, handling safety, and compliance requirements for professional cartridge manufacturing.
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Stainless Steel Needle Material Report
CREDITECH MED uses carefully selected stainless steel materials for tattoo cartridge needle manufacturing. The material composition is verified through professional testing to ensure consistency, stability, and reliable performance during precision needle processing.
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Cartridge Packaging Material Compliance Test
CREDITECH MED verifies packaging material quality through professional testing to ensure safe, stable, and reliable packaging performance for tattoo cartridge needle products.
