Haddenham Venex class 1 (18-21mmHg) armsleeve with grip top and mitten lymphoedema garment long large
Main information
- Trade name:
- Haddenham Venex class 1 (18-21mmHg) armsleeve with grip top and mitten lymphoedema garment long large
- Available from:
- 18-21mmHg
- Class:
- No Controlled Drug Status
- Prescription type:
- Never Valid To Prescribe As A VMP
- Medicine domain:
- Humans
- Medicine type:
- Medical device
Documents
- for the general public:
- The information leaflet for this product is not currently available, you can send a request to our customer service and we will notify you as soon as we are able to obtain it.
Request the information leaflet for the general public.
- for healthcare professionals:
- The information leaflet for this product is not currently available, you can send a request to our customer service and we will notify you as soon as we are able to obtain it.
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Localization
- Available in:
-
United Kingdom
- Language:
- English
Therapeutic information
- Product summary:
- BNF:
Other information
Status
- Source:
- eMC
- Last update:
- 19-02-2019
- The information leaflet for this product is not currently available, you can send a request to our customer service and we will notify you as soon as we are able to obtain it.
Request the information leaflet for the general public.
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19-9-2018
National dietary survey in 2012‐2016 on the general population aged 1‐79 years in the Netherlands
Published on: Tue, 18 Sep 2018 00:00:00 +0200 During the years 2012‐2016, the Dutch National Food Consumption survey was conducted in the Netherlands. For the survey, a random sample was drawn from consumer panels stratified by age and gender and maintained representative to the population with regard to region, address density and educational level. Complete results were obtained for 4,313 persons (response rate 65%); including toddlers, children, adolescents, adults and elderly. Pregnant or lactating ...
Europe - EFSA - European Food Safety Authority Publications
1-6-2018
HeartWare HVAD System by Medtronic: Class I Recall - Due to Unintended Intermittent Electrical Disconnection between the Power Source and the Controller
Interruptions to the electrical connection could cause a pump stop. A pump stop could cause patient harm such as exacerbation of heart failure symptoms, or symptoms such as mild weakness, loss of consciousness, or death.
FDA - U.S. Food and Drug Administration
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