EUDAMED registration B237ZXLATB110NoZephyr Hoverboards & Accessories
- Risk class
- Class I
- CND nomenclatures code
- V080504
- Trade name
- Zephyr Patient Positioning and Transfer System
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- B237ZXLATB110
- Basic UDI
- ++B237HOVERBOARDV7
- Version date
- January 23, 2025
- Manufacturer last update
- August 20, 2024
- Active status
- No
- Manufacturer name
- Diacor Inc.
- Country
- United States
- Country type
- NON_EU
- Address
- 1236 South Airstrip Lane Mount Pleasant
- tami@diacorinc.com
- Name
- E C REP LIMITED
- SRN
- IE-AR-000003995
- Country
- Ireland
- Address
- 5 Fitzwilliam Square East Dublin D2
- info@ecrep.ie
- Telephone
- +353 89 225 1951
- Competent authority
- Health Products Regulatory Authority, Medical Devices Department
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- Germany
- Human tissues
- No
- Animal tissues
- No
PATIENT TRANSFER BOARDS AND TABLES
Access comprehensive regulatory information for Zephyr Hoverboards & Accessories 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 B237ZXLATB110 and manufactured by Diacor Inc. in United States.
This page provides complete registration details including trade name (Zephyr Patient Positioning and Transfer System), manufacturer information, authorized representative details, competent authority (Health Products Regulatory Authority, Medical Devices Department), 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.