Clearblue Ultra early pregnancy tests x2
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Description
CLEAR BLUE
Ultra early pregnancy test
The most sensitive
Detects the pregnancy hormone hCG with a sensitivity of 10 mIU/ml
2 tests
Our most sensitive digital pregnancy test detects the pregnancy hormone hCG with a sensitivity of 10 mIU/ml.
Results as early as 6 days before your period is due to start (i.e. 5 days before your expected period). 78% of pregnancies can be detected 6 days before your period is late, 93% of pregnancies 5 days before and 99% or more from 4 days before your period is late.
Digital "Pregnant" or "Not Pregnant" result in words, so you can be more sure of your early result.
Ergonomic design for a secure grip, an extra-large stem for easy testing, and a unique flashing light to let you know when you've collected enough urine. The test also features unique Floodguard™ Technology, which improves the smooth running of the test. Thanks to our progress indicator, you're reassured throughout the test, until you get your clear digital result in words.
From the presumed date of your period.
How to use it
Always read the instructions carefully before carrying out a test.
If you take the test before the expected date of your period, you should use the first urine of the day. Otherwise, you can take the test at any time during the day. Avoid drinking too much (even water) before using your Digital Ultra Early Detection Pregnancy Test to ensure you don't dilute the hormone levels in your sample.
If you're not sure when to take a test, our digital tool can help you find out when you can take a pregnancy test based on your last period and the length of your cycle.
When you're ready to take the test, remove the test stick from its protective pouch, peel off the blue cap and use the test straight away.
Simply hold the absorbent tip under your urine stream or in a collected urine sample.
Remove the absorbent tip from the urine when the indicator light starts to flash (usually after about 5 seconds). The indicator light will continue to flash briefly and then go out.
Replace the cap and place the digital pregnancy test on a flat surface.
IMPORTANT
During the test, never hold the test stick with the absorbent end pointing upwards.
The progress indicator appears on the screen, and the segments appear in succession to indicate that the test is progressing correctly, counting down to your result
Compositions & ingredients
The composition may be subject to variations, so we advise you to always check the list on the purchased product.
This digital DIV device meets the emission and immunity requirements of EN 61326-2-6. The EMC countermeasures within the electronic instrument provide reasonable protection against the effects of electromagnetic interference likely to be encountered in a domestic environment. The following safety warnings apply to equipment complying with standard EN 61326-2-6. a) Use of this instrument in a dry environment, especially in the presence of synthetic materials (synthetic clothing, carpets, etc.), may cause destructive static discharges which may lead to erroneous results. b) Do not use this instrument near sources of intense electromagnetic radiation (e.g. mobile phones), as these may prevent its ftit. correct operation
For personal use at home. For in vitro diagnostic use only. Not suitable for internal use. Do not reuse. Keep out of reach of Children. Store between 2 and 30°C. If stored in a refrigerator, remove the device and allow it to reach room temperature for 30 minutes before performing the test. Do not use if the protective pouch is damaged. Do not use after the expiry date. This product contains batteries. Dispose of the test in accordance with local regulations. Contains small parts. Do not ingest the components of this device. In the event of accidental ingestion, consult a doctor. Report any injuries caused by the use of this device to Clearblue. SPD Swiss Precision Diagnostics GmbH (SPD), Route de St Georges 47, 1213 Petit-Lancy, Geneva, Switzerland.
Clearblue Ultra Early Detection Digital is a pregnancy test manufactured by SPD Swiss Precision Diagnostics GmBH and distributed by Procter & Gamble Health France SAS. It is recommended that you carry out the test from the date specified in the rules. If you have any doubts about the results obtained, consult your doctor. This in vitro diagnostic medical device is a regulated health product and bears the CE mark. Please read the instructions carefully and seek the advice of a healthcare professional. Internal reference number: 21/02/PROCTER/GP/001. Creation date: 04 February 2021.
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