Cardimed Asia Medikal Sanayi ve Ticaret Ltd Sti
Maltepe, TR
CARDIMED ASIA MEDIKAL SANAYI VE TICARET LTD STI appears in FDA device records in Maltepe, TR. 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 |
|---|---|---|---|---|---|
| 3015453963 | 3015453963 | CARDIMED ASIA MEDIKAL SANAYI VE TICARET LTD STI | Cevizli Mah. Tansel Cad., Maltepe Istanbul 34846 TR | 2026 | and 51 more, listed in full below |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- NBHAccessories, Arthroscopic
- DTLAdaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
- HRXArthroscope
- HTWBit, Drill
- EQJBur, Ear, Nose And Throat
- LITCatheter, Angioplasty, Peripheral, Transluminal
- MQFCatheter, Assisted Reproduction
- KRACatheter, Continuous Flush
- MSDCatheter, Hemodialysis, Implanted
- NYUCatheter, Hemodialysis, Implanted, Coated
- DQOCatheter, Intravascular, Diagnostic
- GBXCatheter, Irrigation
- DQYCatheter, Percutaneous
- QJPCatheter, Percutaneous, Neurovasculature
- NRYCatheter, Thrombus Retriever
- KODCatheter, Urological
- LOXCatheters, Transluminal Coronary Angioplasty, Percutaneous
- FZPClip, Implantable
- NIQCoronary Drug-Eluting Stent
- NIKDefibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)
- HCGDevice, Neurovascular Embolization
- KRDDevice, Vascular, For Promoting Embolization
- ERLDrill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece
- HBEDrills, Burrs, Trephines & Accessories (Simple, Powered)
- GEIElectrosurgical, Cutting & Coagulation & Accessories
- NUJElectrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
- MAIFastener, Fixation, Biodegradable, Soft Tissue
- MBIFastener, Fixation, Nondegradable, Soft Tissue
- HDAForceps, Obstetrical
- LWSImplantable Cardioverter Defibrillator (Non-Crt)
- MDMInstrument, Manual, Surgical, General Use
- HWEInstrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment
- DYBIntroducer, Catheter
- GCJLaparoscope, General & Plastic Surgery
- NLMLaparoscope, General & Plastic Surgery, Reprocessed
- FTLMesh, Surgical, Polymeric
- HBCMotor, Drill, Electric
- HBBMotor, Drill, Pneumatic
- GETMotor, Surgical Instrument, Pneumatic Powered
- HAWNeurological Stereotaxic Instrument
- DQAOximeter
- DPZOximeter, Ear
- OSRPacemaker/Icd/Crt Non-Implanted Components
- NVYPermanent Defibrillator Electrodes
- HTYPin, Fixation, Smooth
- KRGProgrammer, Pacemaker
- NKEPulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)
- NVZPulse Generator, Permanent, Implantable
- KFKSaw, Pneumatically Powered
- HWCScrew, Fixation, Bone
- FPASet, Administration, Intravascular
- GDWStaple, Implantable
- GDTStaple, Removable (Skin)
- GALSuture, Absorbable, Natural
- GAMSuture, Absorbable, Synthetic, Polyglycolic Acid
- GATSuture, Nonabsorbable, Synthetic, Polyethylene
- JKATubes, Vials, Systems, Serum Separators, Blood Collection
- HTNWasher, Bolt Nut
- DQXWire, Guide, Catheter
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