Quipment
Nancy Meurthe-et-Moselle, FR
QUIPMENT appears in FDA device records in Nancy Meurthe-et-Moselle, FR. FDA records list no 510(k) clearances, no PMA records and 2 registered establishments. 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
- 2
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 |
|---|---|---|---|---|---|
| 3008717264 | 3008717264 | QUIPMENT | 269 Rue Julie Victoire Daubie, Nancy Meurthe-et-Moselle 54000 FR | 2026 | and 32 more, listed in full below |
| 3012302888 | 3012302888 | QUIPMENT INC. | 1640 Airport Road, Kennesaw, GA 30144 US | 2026 | and 31 more, listed in full below |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- LIXAid, Cardiopulmonary Resuscitation
- CCKAnalyzer, Gas, Carbon-Dioxide, Gaseous-Phase
- CCJAnalyzer, Gas, Carbon-Monoxide, Gaseous-Phase
- EWOAudiometer
- MKJAutomated External Defibrillators (Non-Wearable)
- HRECabinet, Instrument, Ac-Powered, Ophthalmic
- BXWCalibrator, Volume, Gas
- DLJCalibrators, Drug Specific
- GKGCentrifuge, Hematocrit
- ONBClosed Antineoplastic And Hazardous Drug Reconstitution And Transfer System
- DQKComputer, Diagnostic, Programmable
- FMHContainer, Specimen, Sterile
- FLLContinuous Measurement Thermometer
- LDDDc-Defibrillator, Low-Energy, (Including Paddles)
- GZODevice, Galvanic Skin Response Measurement
- LELDevice, Sleep Assessment
- LASDrug Specific Control Materials
- LBBDynamometer, Ac-Powered
- HRWDynamometer, Nonpowered
- DPSElectrocardiograph
- QDAElectrocardiograph Software For Over-The-Counter Use
- MWJElectrocardiograph, Ambulatory (Without Analysis)
- MLOElectrocardiograph, Ambulatory, With Analysis Algorithm
- DRXElectrode, Electrocardiograph
- HLSExophthalmometer
- BSNFilter, Conduction, Anesthetic
- QDKIntegrated Continuous Glucose Monitoring System For Non-Intensive Diabetes Management
- QBJIntegrated Continuous Glucose Monitoring System, Factory Calibrated
- NQEMicroscope, Specular
- DRTMonitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
- GCBNeedle, Catheter
- DQAOximeter
- DROPacemaker, Cardiac, External Transcutaneous (Non-Invasive)
- JOMPlethysmograph, Photoelectric, Pneumatic Or Hydraulic
- FRNPump, Infusion
- LZHPump, Infusion, Enteral
- MEAPump, Infusion, Pca
- DSFRecorder, Paper Chart
- FRWScale, Patient
- FRIScale, Stand-On, Patient
- FPASet, Administration, Intravascular
- LHISet, I.V. Fluid Transfer
- BZGSpirometer, Diagnostic
- FMFSyringe, Piston
- FFXSystem, Gastrointestinal Motility (Electrical)
- DXNSystem, Measurement, Blood-Pressure, Non-Invasive
- HGMSystem, Monitoring, Perinatal
- KGXTape And Bandage, Adhesive
- GJSTest, Time, Prothrombin
- HKYTonometer, Manual
- DXHTransmitters And Receivers, Electrocardiograph, Telephone
- DRGTransmitters And Receivers, Physiological Signal, Radiofrequency
- JKATubes, Vials, Systems, Serum Separators, Blood Collection
- MNRVentilatory Effort Recorder
- LGZWarmer, Thermal, Infusion Fluid
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