MEDICAL CLEARANCE FORM (MEDA) This form is intended to provide CONFIDENTIAL information to enable the airline's MEDICAL Department to assess the fitness of the passenger to travel. If the passenger is acceptable for air travel, this information will permit the issuance of the necessary directives ...
After reviewing your special assistance form, we may request medical clearance via the medical information form to make sure air travel is completely safe for you. You should carefully fill in both pages of the form. Please follow these steps: Complete the medical information form part 1 by you...
Apply for medical clearance Read ourguidelinesto understand how we determine if you’re medically fit to fly. If you need to apply for medical clearance, please complete aMEDIF form If you require a wheelchair, please request one at least 48 hours before your flight. We may not be able to...
Most people with existing medical conditions are able to fly without difficulty. However, sometimes certain precautions need to be taken andin some cases, we might request medical clearance. If you are travelling with pre-existing medical conditions an...
A particularly severe form of anemia is sickle cell disease, which may be exacerbated by reduced oxygen pressures. Because such a crisis could be life-threaten- ing, such patients should be advised not to travel by air without medical oxygen. Sickle cell trait, on the other hand, has not...
ContactAsia Actualwith questions or a request for support in Thailand. Asia Actual has a fully licensed offices in Bangkok staffed by experienced, bi-lingual regulatory and commercial professionals to offer medical device registration, independent license holding, importing and sales support services in ...
Work with legal, regulatory, commercial, trade compliance, freight forwarders, and local customs authorities in Indonesia to ensure all customs clearance procedures are compliant with regulations. Determine the necessary workforce and skills required to support the go-to-market strategy and build a team...
The 1976 federal law that mandated safety testing for high-risk medical devices also created a far easier — and less costly — pathway to the marketplace. This process, known as a 510(k) clearance, requires manufacturers to show a new device they plan to sell has "substantial equivalence...
This was done after distributing the form to 30 participants first, and recording their responses and feedback to see how each participant interpreted the question. Their feedback, if any, was considered when making changes to the questionnaire based on this pilot experiment. The questionnaire ...
• A few Class I and Most Class II medical devices must be reviewed by the FDA through a 510(k) clearance before they can be made available for sale in the U.S. Many of these devices are cleared for prescription-only use or use only in health care ...