Compatible GE DINAMAP V100 Vital Signs Monitor SpO₂ Sensor

Compatible GE DINAMAP V100 Vital Signs Monitor SpO₂ Sensor is supplied as a compatible spo₂ sensor for patient monitor and pulse oximetry applications. This fast baseline page keeps the original product references while presenting the item in a cleaner structure for buyers, engineers, and distributors.

Compatible GE DINAMAP V100 Vital Signs Monitor SpO₂ Sensor

Product Details

Product type SpO₂ sensor
Application Patient monitor SpO₂ measurement and accessory replacement
Available styles Adult, pediatric, neonate, clip, soft-tip, wrap, or multi-site styles may be available depending on model
Cable / connector Refer to the product image and original compatibility notes before ordering
Supply note Compatible replacement item; original brand names and part numbers are used only to identify compatibility

Compatibility and Ordering Notes

compatible GE DINAMAP V100 vital monitor SpO₂ sensor SpO₂ products >> compatible GE DINAMAP V100 vital monitor SpO₂ sensor compatible GE Medical DINAMAP V100 masimo SpO₂ sensors adult, pediatric, neonate are available clip, soft gloves, wrap type are available detachable, integrated sensors are available. disposable, reusable are available compatible GE Medi

compliance with EN60601-1 ISO80601-2-61 ISO 10993-1 ISO 10993-5 ISO 10993-10

compliance with RoHS Follow us on Facebook compatible GE Marquette three/five lead ECG trunk cable compatible GE Ohmeda SpO₂ sensor OXY-F4-MC compatible GE Marquette Dash Solar Eagle series one piece three lead ECG cable with leadwire neonate clip compatible GE Datex OXY-F4-N SpO₂ sensor compatible GE Hellige Generation ECG cable compatible GE TS-F-D TS-E-D

Please confirm the monitor model, connector shape, patient size, sensor style, and required cable length before ordering. If the original part number or connector photo is available, send it to Pan-SW Med for cross-checking.

Compliance and Use Notice

Products are supplied for professional medical equipment maintenance and accessory replacement. Compatibility descriptions are for identification only. Final use should follow the device manufacturer’s instructions and the buyer’s clinical engineering requirements.