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Depending on your market: EU CE MDR, US FDA, UK UKCA, Australia TGA, Germany DIN, and US OSHA for workplace kits. We adjust contents, provide registration documents, SDS and test reports, and handle compliant declaration throughout.
Key points:
1. EU: CE MDR - Technical file plus EU Authorised Representative and EUDAMED registration.
2. US: FDA - Device registration and labeling rules per FDA requirements.
3. UK: UKCA - Independent UK conformity assessment after Brexit.
4. DE / US workplace - DIN 13164 for German vehicle kits and ANSI/OSHA for US workplace kits.
We design multi-certification compatible kits so one configuration can satisfy several markets at once.
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