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NeoBeat

Newborn Heart Rate Meter

Clinical Evidence

6

Available clinical studies

 

View Clinical Evidence

 

Prevalence of bradycardia in 4876 newborns in the first minute after birth and association with positive pressure ventilation: a population-based cross-sectional study​

Year
2024
Author
Rettedal et al.
Journal
Arch Dis Child Fetal Neonatal Ed
Publication Details
2024 Jun 19;109(4):371-377

 


 

Newborns requiring resuscitation: Two thirds have heart rate ≥100 beats/minute in the first minute after birth​

Year
2023
Author
Kibsgaard et al.
Journal
Acta Paediatrica
Publication Details
2023 Apr;112(4):697-705​

 


 

​Comparing pulse rate measurement in newborns using conventional and dry-electrode ECG monitors

Year
2022
Author
van Twist et al.
Journal
Acta Paediatrica
Publication Details
2022 Jun;111(6):1137-1143​

 


 

​NeoBeat offers rapid newborn heart rate assessment

Year
2021
Author
Bush et al.
Journal
Arch Dis Child Fetal Neonatal Ed
Publication Details
2021 Sep;106(5):550-552​

 


 

​Heart rate detection properties of dry-electrode ECG compared to conventional 3-lead gel-electrode ECG in newborns

Year
2021
Author
Pike et al.
Journal
BMC Res Notes
Publication Details
2021 May 1;14(1):166

 


 

​​Comparison of Heart Rate Feedback from Dry-Electrode ECG, 3-Lead ECG, and Pulse Oximetry during Newborn Resuscitation

Year
2021
Author
Rettedal et al.
Journal
Children
Publication Details
2021 Nov 26;8(12):1092

Technical Specifications

Dimensions: NeoBeat: 83 x 87 x 40 mm (3.2 x 3.4 x 1.6 inches)
NeoBeat Mini: 70 x 70 x 40 mm (2.8 x 2.8 x 1.6 inches)
Weight: NeoBeat: 31 g (1.1 oz)
NeoBeat Mini: 27 g (1 oz)
Applied Materials: Polyamide, thermoplastic polyurethane, stainless steel

Regulatory Standards and Approvals

​Europe: CE marked as class IIa device in accordance with Council Directive 93/42/EEC Medical Device Directive, as amended by Council Directive 2007/47/EC.​

USA: 501(k) FDA clearance as Class 2 device​

Laerdal Medical AS is certified by DNV Product Assurance AS to ISO 13485:2016, including the regulatory requirements of the MDSAP member states, Australia, Brazil, Canada, Japan and USA.

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