8 results
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73ms
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Sources: EU EUDAMED, US FDA
FIRST MEDICAL SOURCE, LLC
FDA registration
FIRST MEDICAL SOURCE, LLC·2 products·🇺🇸 United States
First Medical Source (FMS)
FDA UDI
First Medical Source, LLC·00851111007101·Single 5" (30 holes) FMS Conduction Catheter Kit
First Medical Source (FMS)
FDA UDI
First Medical Source, LLC·00851111007002·Dual 5" (30 holes) FMS Conduction Catheter Kit
INFULIFE INFUSION PUMP
FDA Adverse Event
Malfunction
·FIRST MEDICAL SOURCE, LLC·Product code MEB·December 5, 2025
EASY PUMP
FDA Adverse Event
Malfunction
·FIRST MEDICAL SOURCE, LLC·Product code MEB·December 8, 2025
Medpro Elastomeric Infusion Pump. AccuFlux, Model # CT-0020-100H. Product Usage: The devices are intended for patients requiring intravenous, percutaneous, subcutaneous, intra-operative sites or epidural administration of medications. It is the responsibility of the user to ensure that the medication is prepared and administered accordance with the drug manufacturers package insert. The devices deliver controlled amounts of medication directly to the intraoperative site for pain management and or antibiotic administration. The devices infuse the medication at an hourly flow rate. Medications are infused intraoperatively and postoperatively through intramuscular or subcutaneous routes. The devices are also intended for controlled delivery of local anesthetics in close proximity to nerves for post operative regional anesthesia and pain management. Routes of administration may be intraoperative or percutaneous. It is for continuous infusion of medications for general infusion use, including antibiotic delivery and chemotherapy.
FDA Recall
Terminated
·First Medical Source LLC·Product code MEB·July 9, 2011
Medpro Elastomeric Infusion Pump. AccuFlux, Model # CT-0020-100H. Product Usage: The devices are intended for patients requiring intravenous, percutaneous, subcutaneous, intra-operative sites or epidural administration of medications. It is the responsibility of the user to ensure that the medication is prepared and administered accordance with the drug manufacturers package insert. The devices deliver controlled amounts of medication directly to the intraoperative site for pain management and or antibiotic administration. The devices infuse the medication at an hourly flow rate. Medications are infused intraoperatively and postoperatively through intramuscular or subcutaneous routes. The devices are also intended for controlled delivery of local anesthetics in close proximity to nerves for post operative regional anesthesia and pain management. Routes of administration may be intraoperative or percutaneous. It is for continuous infusion of medications for general infusion use, including antibiotic delivery and chemotherapy.
FDA Enforcement
Class I
·Terminated·First Medical Source LLC·December 5, 2012
VMX MOBILE X-RAY SYSTEM
FDA Adverse Event
Malfunction
·GE MEDICAL SYSTEMS, LLC·Product code IZL·February 13, 2012