CENTERPIECE S. de R.L de C.V (sterilization site)
Tijuana Baja California, MX
CENTERPIECE S. DE R.L DE C.V (sterilization site) appears in FDA device records in Tijuana Baja California, 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 |
|---|---|---|---|---|---|
| 3019807891 | 3019807891 | CENTERPIECE S. DE R.L DE C.V (sterilization site) | Bulevar La Encantada Industrial, Parque Industrial El Florido, Seccion La Encantada #11530, Tijuana Baja California 22250 MX | 2026 | and 77 more, listed in full below |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- KRIAccessory Equipment, Cardiopulmonary Bypass
- DTLAdaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
- CACApparatus, Autotransfusion
- EXFBag, Bile Collecting
- EOQBronchoscope (Flexible Or Rigid)
- LPBCardiac Ablation Percutaneous Catheter
- DWFCatheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
- KRACatheter, Continuous Flush
- DRFCatheter, Electrode Recording, Or Probe, Electrode Recording
- DQOCatheter, Intravascular, Diagnostic
- DQYCatheter, Percutaneous
- DRACatheter, Steerable
- LOXCatheters, Transluminal Coronary Angioplasty, Percutaneous
- DXCClamp, Vascular
- DTQConsole, Heart-Lung Machine, Cardiopulmonary Bypass
- DWAControl, Pump Speed, Cardiopulmonary Bypass
- GXRCover, Burr Hole
- DTPDefoamer, Cardiopulmonary Bypass
- DREDilator, Vessel, For Percutaneous Catheterization
- LHGElectrode, Spinal Epidural
- MAIFastener, Fixation, Biodegradable, Soft Tissue
- MBIFastener, Fixation, Nondegradable, Soft Tissue
- DTRHeat-Exchanger, Cardiopulmonary Bypass
- DXTInjector And Syringe, Angiographic
- KNWInstrument, Biopsy
- DYBIntroducer, Catheter
- HETLaparoscope, Gynecologic (And Accessories)
- DRYMonitor, Blood-Gas, On-Line, Cardiopulmonary Bypass
- DTZOxygenator, Cardiopulmonary Bypass
- HRSPlate, Fixation, Bone
- KWYProsthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
- LZOProsthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
- JDIProsthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
- LPHProsthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
- KWSProsthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented
- KFMPump, Blood, Cardiopulmonary Bypass, Non-Roller Type
- DTNReservoir, Blood, Cardiopulmonary Bypass
- HWCScrew, Fixation, Bone
- DZLScrew, Fixation, Intraosseous
- LKNSeparator, Automated, Blood Cell And Plasma, Therapeutic
- GKTSeparator, Automated, Blood Cell, Diagnostic
- FPASet, Administration, Intravascular
- JDRStaple, Fixation, Bone
- EZWStimulator, Electrical, Implantable, For Incontinence
- MHYStimulator, Electrical, Implanted, For Parkinsonian Tremor
- GZFStimulator, Peripheral Nerve, Implanted (Pain Relief)
- GZBStimulator, Spinal-Cord, Implanted (Pain Relief)
- LGWStimulator, Spinal-Cord, Totally Implanted For Pain Relief
- GASSuture, Nonabsorbable, Synthetic, Polyester
- GATSuture, Nonabsorbable, Synthetic, Polyethylene
- GAWSuture, Nonabsorbable, Synthetic, Polypropylene
- FMFSyringe, Piston
- KSWSystem, Processing For Frozen Blood
- KGXTape And Bandage, Adhesive
- JKATubes, Vials, Systems, Serum Separators, Blood Collection
- FPKTubing, Fluid Delivery
- DWETubing, Pump, Cardiopulmonary Bypass
- FGBUreteroscope And Accessories, Flexible/Rigid
- DSQVentricular (Assist) Bypass
- HTNWasher, Bolt Nut
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
