TMS Litters
- Risk class
- Class I
- CND nomenclatures code
- V08050103
- Trade name
- FOXTROT LITTER AND CARRIER- DA (RESCUE ORANGE)
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 00818630014027
- Basic UDI
- 081863001TMSLittersLW
- Version date
- September 12, 2024
- Manufacturer last update
- June 24, 2024
- Active status
- No
- Manufacturer name
- TacMed Solutions, LLC
- Country
- United States
- Country type
- NON_EU
- Address
- 1250 Harris Bridge Road Anderson, South Carolina
- info@tacmedsolutions.com
- SRN
- NL-AR-000037688
- Country
- Netherlands
- Address
- 2b Lange Viestraat Utrecht
- eurep@casusconsulting.com
- Competent authority
- Ministerie van Volksgezondheid, Welzijn en Sport
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- Germany
- Market available
- Belgium:None~None, Bulgaria:None~None, Croatia:None~None, Cyprus:None~None, Czechia:None~None, Denmark:None~None, Estonia:None~None, Finland:None~None, France:None~None, Germany:None~None, Greece:None~None, Hungary:None~None, Ireland:None~None, Italy:None~None, Lithuania:None~None, Luxembourg:None~None, Netherlands:None~None, Norway:None~None, Poland:None~None, Portugal:None~None, Romania:None~None, Slovakia:None~None, Spain:None~None, Sweden:None~None, United Kingdom (Northern Ireland only):None~None
- Human tissues
- No
- Animal tissues
- No
EMERGENCY AND TRAUMATOLOGY STRETCHERS
Access comprehensive regulatory information for TMS Litters in the European Union medical device market through Pure Global AI's free database. This Class I device is registered with EU EUDAMED under Primary DI 00818630014027 and manufactured by TacMed Solutions, LLC in United States.
This page provides complete registration details including trade name (FOXTROT LITTER AND CARRIER- DA (RESCUE ORANGE)), manufacturer information, authorized representative details, competent authority (Ministerie van Volksgezondheid, Welzijn en Sport), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.