Bendable Armboard
- Risk class
- Class I
- CND nomenclatures code
- C010180
- Trade name
- Dale Bendable Armboard
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 00817612020322
- Basic UDI
- 0817612026526W
- Version date
- March 09, 2022
- Manufacturer last update
- January 17, 2022
- Active status
- No
- Manufacturer name
- Dale Medical Products, Inc.
- Country
- United States
- Country type
- NON_EU
- Address
- 40 Kenwood Circle 02038 Franklin
- r.gruneberg@dalemed.net
- Name
- MDSS GmbH
- SRN
- DE-AR-000005430
- Country
- Germany
- Address
- 41 Schiffgraben Hannover
- info@mdssar.com
- Competent authority
- DE/CA09 - Staatliches Gewerbeaufsichtsamt Hannover
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- Germany
- Market available
- Austria:None~None, 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, Iceland:None~None, Ireland:None~None, Italy:None~None, Latvia:None~None, Liechtenstein:None~None, Lithuania:None~None, Luxembourg:None~None, Malta:None~None, Netherlands:None~None, Norway:None~None, Poland:None~None, Portugal:None~None, Romania:None~None, Slovakia:None~None, Slovenia:None~None, Spain:None~None, Sweden:None~None, Turkey:None~None, United Kingdom (Northern Ireland only):None~None
- Human tissues
- No
- Animal tissues
- No
PERIPHERAL I.V. CATHETERS AND CANNULAS - ACCESSORIES NOT INCLUDED IN OTHER CLASSES
Access comprehensive regulatory information for Bendable Armboard 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 00817612020322 and manufactured by Dale Medical Products, Inc. in United States.
This page provides complete registration details including trade name (Dale Bendable Armboard), manufacturer information, authorized representative details, competent authority (DE/CA09 - Staatliches Gewerbeaufsichtsamt Hannover), 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.