Plexus Electronica S. de R.L. de C.V.
Zapopan Jalisco, MX
Plexus Electronica S. de R.L. de C.V.. appears in FDA device records in Zapopan Jalisco, MX. FDA records list no 510(k) clearances, no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
- 510(k) clearances
- 0
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 1
510(k) clearance history
No 510(k) clearance records for this company in the ingested FDA data.
No 510(k) clearance records in the ingested FDA data.
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3011120183 | 3011120183 | Plexus Electronica S. de R.L. de C.V.. | Paseo del Norte #4640, Zapopan Jalisco 45010 MX | 2026 | and 26 more, listed in full below |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- CCKAnalyzer, Gas, Carbon-Dioxide, Gaseous-Phase
- OLZAutomatic Event Detection Software For Polysomnograph With Electroencephalograph
- MCXCatheter, Coronary, Atherectomy
- OAECatheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
- OADCatheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter
- NZUCollector, Urine, Powered, Non Indwelling Catheter
- MNTContinuous, Minimal Ventilatory Support, Facility Use Ventilator
- NOUContinuous, Ventilator, Home Use
- LWHCounter, Sponge, Surgical
- DSIDetector And Alarm, Arrhythmia
- NHJDevice, Positive Pressure Breathing, Intermittent
- KZADevice, Vein Location, Liquid Crystal
- HGIElectrocautery, Gynecologic (And Accessories)
- GEIElectrosurgical, Cutting & Coagulation & Accessories
- CAWGenerator, Oxygen, Portable
- BZEHeater, Breathing System W/Wo Controller (Not Humidifier Or Nebulizer
- BTTHumidifier, Respiratory Gas, (Direct Patient Interface)
- LWSImplantable Cardioverter Defibrillator (Non-Crt)
- LFLInstrument, Ultrasonic Surgical
- QBJIntegrated Continuous Glucose Monitoring System, Factory Calibrated
- SDTIntra-Pulmonary Percussive Vibration (Ipv) Devices
- CCWLaryngoscope, Rigid
- MHXMonitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
- OSRPacemaker/Icd/Crt Non-Implanted Components
- BYIPercussor, Powered-Electric
- QZIPercutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation
- NVYPermanent Defibrillator Electrodes
- KRGProgrammer, Pacemaker
- NVZPulse Generator, Permanent, Implantable
- GKTSeparator, Automated, Blood Cell, Diagnostic
- OLVStandard Polysomnograph With Electroencephalograph
- KGXTape And Bandage, Adhesive
- CBKVentilator, Continuous, Facility Use
- MNSVentilator, Continuous, Non-Life-Supporting
- BZDVentilator, Non-Continuous (Respirator)
- MNRVentilatory Effort Recorder
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain
