Respicardia

US Last updated 23 Oct 2026

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Devices: 12
Registries: GUDIDFDA PMAFDA
FDA recalls: 0

Catalogue12

respistim R Stimulation Lead, Inline Connector 3602 Ref 3602

Class III FDA UDI Active
Lead Test Adaptor, remede EL-X 1007 Ref 1007

Class III FDA UDI Active
respistim LQS Stimulation Lead, Inline Connector 4685 Ref 4685

Class III FDA UDI Active
respistim R Stimulation Lead, Inline Connector 3652 Ref 3652

Class III FDA UDI Active
respistim LQS Stimulation Lead, Inline Connector 4665 Ref 4665

Class III FDA UDI Active
remede EL/EL-X External Pulse Generator 1006A Ref 1006A

Class III FDA UDI Active
respistim R Stimulation Lead, Inline Connector 3603 Ref 3603

Class III FDA UDI Active
remede EL-X System Implantable Pulse Generator Inline Connector 1600 Ref 1600

Class III FDA UDI Active
respistim LQS Stimulation Lead, Additional Proximal Tubing 4165 Ref 4165

Class III FDA UDI Active
respistim R Stimulation Lead, Inline Connector 3653 Ref 3653

Class III FDA UDI Active
remede EL System Implantable Pulse Generator IS-1 1100 Ref 1100

Class III FDA UDI Active
remede® System Ref P160039

Class III FDA PMA Active

Information

Country: US
Address: 12400 Whitewater Dr Ste 150, Minnetonka, MN, 55343
FDA FEI number: 3009144177