The element helium (He) was discovered 1868 when P.J.C. Janssen and N. Lockyer detected a new line in the solar spectrum during the solar eclipse. Lockyer and E. Frankland suggested the name helium (Gr. Helios, the sun) for the new element. In 1895, helium was discovered in the uranium mineral cleveite and in 1907 it was found out that alpha particles are helium nuclei.
Properties: Helium belongs to the noble gases, is colorless, odorless, and occurs in two naturally isotopes, helium 3 and helium 4. As an inert gas, helium does not react chemically largely and don't burns. Helium 4 makes up over 99% of naturally occurring helium atoms. Helium is extracted from natural gas e.g. present in various radioactive minerals as a decay product. Deposits and sources are in the USA, Poland, the USSR, and a few in India. The rare deposits and increased consumption lead to a shortage of this gas.
K. Onnes worked for many years to liquefy helium, which persisted as a gas to the lowest temperature. Helium does not freeze at atmospheric pressure. The density of helium vapor at his boiling point of 4.2 Kelvin is very high, with the vapor expanding greatly when heated to room temperature. Nb, Tc, Pb, La, V, and Ta are superconductors at liquid helium temperature. Liquid helium is commonly used as a cryogen for superconducting magnets. A rapid evaporation of the cryogen is named Quench. See also Quenching.

Cryogenic liquids and their associated cold vapors can produce effects on the skin similar to a thermal burn and can cause frostbite. Prolonged breathing of extremely cold gases may damage the lungs and in absence of enough air or oxygen, asphyxiation and death can occur. Unprotected skin can stick to very cold metal (e.g. cooled by liquid helium) and then tear when pulled away.

Not necessarily a contraindication, but the examination may damage or impair it. An insulin pump can be disconnected easily for a period of time. Remove the pump while outside the 5 Gauss line, because the pump batteries and motor are magnetic.

Most of the commonly used intrauterine contraceptive devices (IUD) do not move under the influence of the magnetic field, do not heat up during sequences usually applied for pelvic imaging, and do not produce major artifacts in vitro or in vivo.

Thus, patients with either all plastic or copper IUDs can be safely imaged with magnetic resonance imaging (MRI) machines.

The owner of MRI equipment has to ensure that the equipment does fulfill the local requirements.
In some countries, the requirements are more stringent than in others; in other countries, they are nonexistent.
The user in general is unable to check power output, gradient strength, or even field strength. The manufacturer has to cover authorized hardware and software updates after the initial installation and has to give guarantee for the requirements. Specially designed computer programs usually supervise the power output of MRI devices and will not allow or will interrupt any imaging or spectroscopy procedure exceeding those limits considered safe.

See also European Medicines Agency, FDA information:
www.fda.gov/cdrh/safety/mrisafety.html

If a device is to be labeled MR Safe, the following information should be provided:
If a device is to be labeled MR Compatible, the following information should be provided:
Test Conditions:
The static magnetic field strength (Gauss (G) or Tesla (T)) to which the device was tested and demonstrated to be MRI 'safe', 'compatible', or 'intended for use in' should be related to typical machine ratings (e.g. 0.5 T, 1.5 T, 2.0 T, and shielded or unshielded magnet, etc).
The same conditions should be used for the spatial gradient (field strength per unit distance (i.e., G/cm)) in which the device was tested and demonstrated to be 'safe', 'compatible', or 'intended for use in'.
Also the RF transmitter power used during testing of the device, should be related to this typical machine ratings.