Legal

MediTime Pro is a Class I medical device. Manufacturer: , . Software version . Full device details are on the Device information screen.

What this app is

MediTime Pro records the times at which you tell it that doses of paracetamol or ibuprofen have been taken, for up to five people, and shows the time until the next dose would be due under the standard over-the-counter limits.

It is a record and timing aid. It does not give medical advice, does not diagnose, does not decide doses, and does not detect or prevent an overdose. It does not replace advice from a doctor or pharmacist. If you have been given a dosing schedule that differs from the packet, follow the one you were given.

Limits you need to know about

The app only knows about doses you record. A dose given and not recorded will make the app show a longer gap than there really was.
Records are deleted automatically once they are more than 24 hours old. There is no history and nothing to export.
Records are held on this device only. Clearing browser data deletes them.
The built-in limits govern timing and number of doses, not amount. They are the standard over-the-counter limits and apply to adults and children alike. The amount in each dose is on the packet and, for a child, depends on age and weight. The app never checks it.
The counts are wrong for prescription-strength products and for combination medicines containing paracetamol or ibuprofen.

The full list of warnings is on the Device information screen.

Terms of use

Your use of the app is governed by the terms you accepted when you first opened it. You can read them again at any time on the Agreement screen. Those terms include our liability position and your statutory rights.

Reporting a problem

If the app behaved in a way that could have led to harm, tell us using the contact details on the Device information screen. You can also report a problem with a medical device to the MHRA through the Yellow Card scheme at yellowcard.mhra.gov.uk.

In an emergency

If you think too much has been taken, do not wait for symptoms to appear. Contact NHS 111, or call 999 if the person is unwell. Take the packet with you.

Changed on purpose. The previous version of this page asked users to indemnify the developer against all claims and disclaimed all liability. Against a consumer that is unenforceable, and for a registered medical device manufacturer it also sits badly next to the duty to investigate complaints. The liability position now lives in one place, the agreement, where a solicitor can review it as a whole. This page states what the device is and what it cannot do, which is what it needs to do under Path B.