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Neonate Dual Tube Blood Pressure Cuff

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Neonate Dual Tube Blood Pressure Cuff

Neonate Dual Tube Blood Pressure Cuff from PanSW Medical, a compatible reusable nibp cuff for GE Medical Systems Dash, Eagle, Datex-Ohmeda and other compat

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Product information

Neonate Dual Tube Blood Pressure Cuff

Reusable neonate dual tube blood pressure cuff for compatible patient monitoring systems. Designed for small limb sizes with dual hoses and a compact cuff structure for neonatal NIBP measurement.

Product typeReusable NIBP cuff
Part / referenceNeonate dual tube cuff
CompatibilityGE Medical Systems Dash, Eagle, Datex-Ohmeda and other compatible dual tube NIBP systems
Supply useReplacement, repair and accessory assembly

Neonate Dual Tube Blood Pressure Cuff

Product Description

Reusable neonate dual tube blood pressure cuff for compatible patient monitoring systems. Designed for small limb sizes with dual hoses and a compact cuff structure for neonatal NIBP measurement.

PanSW Medical supplies compatible NIBP cuffs, hoses and connectors for patient monitor maintenance, distributor stock and replacement accessory projects. For accurate matching, please confirm the monitor model, connector style, tube configuration and required size before order confirmation.

Specifications

  • Arm circumference range: 6 cm to 11 cm
  • Dual tube design
  • Tube length: 30 cm
  • Compatible with GE Medical Systems Dash, Eagle, Datex-Ohmeda and other dual tube NIBP systems; confirm connector before ordering

Applications and Order Notes

This item is intended for compatible NIBP accessory replacement or assembly use. Please provide photos of the original connector, cuff label, hose end or monitor socket if the exact version is uncertain.

  • Check single tube or dual tube configuration before ordering.
  • Confirm cuff size, hose length, connector type and patient group.
  • For OEM-style orders, sample confirmation is recommended before bulk production.

Image Gallery

Compliance and Safety Notes

Materials and production can be supplied according to applicable medical accessory requirements such as ANSI/AAMI SP10, EN60601-1, ISO 10993 related biocompatibility evaluation and RoHS where applicable. Final compatibility and clinical use should be verified by qualified biomedical or purchasing personnel.

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