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A postpartum pad that absorbs and quantifies blood in real time.

No more visual estimations and late detection, ensuring a solution to monitor and manage PPH globally. An innovative Class I medical device to change maternal care worldwide.

A breakthrough in postpartum care

· The Pad

Designed to do more than just absorb blood, the Nataly Pad accurately measures it in real time. It is intended for the critical first 24 hours after childbirth, when PPH risk peaks. With Nataly, postpartum bleeding is no longer a guess — it's measurable.

In Hospitals

Midwives can ensure timely detection of a hemorrhage.

At Home

Ideal for home births or postpartum recovery after hospital discharge.

A box of Nataly postpartum pads with blood loss quantification system, containing 20 superabsorbent pads for postpartum bleeding measurement.

Device characteristics

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Accessible

Cost-effective

Easy to use

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Non-invasive

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Non-electronic

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Rapid deployment

Easy, quick and reliable

· How it works

Nataly is designed to act fast. Used right after childbirth, it enables midwives to easily quantify blood loss, detect postpartum hemorrhage early, and ensure timely interventions to reduce health complications and costs.

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Nataly is placed after delivery

Each pad absorbs up to 300 mL of blood. It’s worn during the first 24 hours and replaced as needed.

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Midwives monitor blood loss

Blood loss is visible from the outside of the pad, and if it reaches 500 mL at any point, the PPH protocol is activated immediately.

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Early treatment is given

Timely pharmacological treatment reduces risks, preventing complications and lowering healthcare costs.

A small cost for a big impact

We bring measurable improvements to maternal care, saving lives, reducing costs, and simplifying clinical response

42k

lives could be saved yearly*, assuming 90% detection accuracy

$10k

in direct hospital costs saved for each avoided >1L blood loss case*

2x

reduction in pad usage compared to standard PPH workflows

85%

faster detection compared to visual estimation alone

5x

reduction in uterotonic drug use enabled by earlier detection

<30

seconds to activate PPH protocol enabling a faster response

* Data from the E-MOTIVE randomized trial (Draper et al., 2023) involving over 200,000 women.