Questions about remedē?

The Patient Manual

is designed to give you the information you need to feel comfortable and confident with your therapy.

remedē Patient Manual

To address common question, and in accordance with Medical Device Regulation (MDR) Articel 18, we direct you to the following information:

Patient Manual Page 5, Section 7.0	Warning: Things you must do to avoid serious harm
Patient Manual Page 7, Section 8.0	What happens when the remedē System wears out
Patient Manual Page 8, Section 9.0	Risks of using this device
See device specification tables below	Device specification and material exposures

Device Specifications

remede^® System IPG (Modell 1001) Physical Description
Height	80 mm
Length	47.5 mm
Thickness	14.6 mm
Volume	39 cm³
Mass	64 g
Materials exposed to tissue	Titanium, epoxy resin, silicone rubber

remedē System IPG (Modell 1001) Battery Information
Chemistry	Lithium Carbon Monofluoride (WG 9086)
Nominal Voltage	2.9 – 2.95 Volts (at 37 °C)
Capacity	2.2 Amp-hours (Ah)
Elective Replacement Indicator (ERI)	2.60 Volts
End of Life (EOL)	2.50 Volts

respistim® LQS Stimulation Lead Specifications Electrodes
Material	Platinum/Iridium
Electrode Surface Area	12 millimeters²
Coating	None
Steroid	None

Terminal
Compatibility	IS-1.
Material	316L Stainless Steel

Conductors
Type	Co-radial design, hexafilar coil with coated wire

respistim R Lead Specifications Electrodes
Material	Platinum/Iridium
Electrode Surface Area	29 millimeters²
Coating	None
Steroid	None

Terminal
Compatibility	IS-1.
Material	316L Stainless Steel

Conductors
Type	Co-radial design, hexafilar coil with coated wire

respistim R Model Descriptions

Model	Length (centimeter)	Distal helical Spring Length (millimeters)	Distal Helical Spring Diameter (millimeters)
3101	60	25	20
3102	60	25	24
3103	60	35	20
3104	60	35	24
3105	60	45	20
3106	60	45	24
3201	80	25	20
3202	80	25	24
3203	80	35	20
3204	80	35	24
3205	80	45	20
3206	80	45	24