Immobilisation bandages
- Risk class
- Class I
- CND nomenclatures code
- M030501
- Trade name
- Arm Sling
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 00840270622393
- Basic UDI
- 08402706CL1014K
- Active status
- No
- Manufacturer name
- OPPO Medical Inc.
- Country
- United States
- Country type
- NON_EU
- Address
- Ste. 220080 Seattle City Center, 1420 Fifth Ave. Seattle
- brittanywang@oppomedical.com
- SRN
- DE-AR-000000085
- Country
- Germany
- Address
- 7 Ernst-Heckel-Straße St. Ingbert
- ear@mt-procons.com
- Telephone
- +49 6894 581020
- Competent authority
- DE/CA70 - Landesamt für Umwelt- und Arbeitsschutz
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- Poland
- Market available
- Bulgaria:None~None, Croatia:None~None, Cyprus:None~None, Czechia:None~None, Greece:None~None, Italy:None~None, Latvia:None~None, Malta:None~None, Poland:None~None, Portugal:None~None, Slovakia:None~None
- Human tissues
- No
- Animal tissues
- No
IMMOBILISATION BANDAGES FOR SHOULDER, ARM AND COLLARBONE
Access comprehensive regulatory information for Immobilisation bandages 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 00840270622393 and manufactured by OPPO Medical Inc. in United States.
This page provides complete registration details including trade name (Arm Sling), manufacturer information, authorized representative details, competent authority (DE/CA70 - Landesamt für Umwelt- und Arbeitsschutz), 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.