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  • Natrix Intestinal Wellbeing Area Faeces and Urine Collection and Transport Kit

Natrix Intestinal Wellbeing Area Faeces and Urine Collection and Transport Kit

21.37€
  • Brand: NATRIX Srl
  • Product Code: 970538397
  • EAN:
  • Availability: In 10 - 14 Days
  • Purchase 3 items for 20.94€ each
  • Purchase 4 items for 20.52€ each
  • Purchase 5 items for 20.09€ each
Price information ⓘ

Natrix

Intestinal Wellness Area

Feces and Urine Collection and Transport Kit

Description
Kit containing material for the collection and transport of biological sample faeces eurine.

Test possible
The biological sample collected can be used to perform the tests: Dysbiocheck, Proflora check, Parasitology check, Inflammation check, Digestion check and Permeability check.

Packaging
Cardboard case with colored identification band.

Content
1 sterile Vacutainer urine collection tube.
1 shipping container (yellow cap) urine.
2 sterile stool collection tubes.
3 shipping container (brown) feces.
2 ESWAB collection kit A tubes.
1 Minisystem Paragreen parasitological test tube.
5 white labels.
4 package leaflets.

storage
Store at room temperature.
Keep away from sources of heat, sunlight and humidity.

Stability
5 years and in any case no later than the expiry date indicated on the package.

Warnings
Do not use beyond the expiration date.
All patient samples must be properly disposed of.
Do not reuse.
The integrity of the packaging and kit components guarantees the sterility of the sterile components.
The packages must be opened only at the moment of use.

Do not use if package is damaged before opening.

The product is compliant:
• the directive relating to in vitro diagnostic medical devices 98/79 / EC recognized in Italy by Legislative Decree No. 332 of 08/09/2000;
• UNI CEI EN ISO 14971: 2012: Medical devices - Application of risk management to medical devices;
• to all the essential safety requirements that concern them and to all the requirements dictated by the mandatory standards.
The in vitro diagnostic medical device belongs, according to point 9 of Legislative Decree 332/2000, to the fourth category of devices (in vitro-diagnostic medical device).