FEI 3010041511Initial importer
Teleflex Llc (nadc)
11245 N Distribution Cove, Olive Branch, MS, US
MDR events19All time
Recalls0All time
Registered products463
Establishment typeRepackRepack or Relabel Medical Device
Registered product codes
463 product codes
Recent MDR events
19 on file
- AC3 OPTIMUS(TM) IABPJul 16, 2026InjuryMW5190739
- AC3 OPTIMUS IABP CONSOLEMay 7, 2026MalfunctionMW5187864
- CATHETER, INTRAVASCULAR, THERAPEUTIC, LONG-TERM GREATER THAN 30 DAYSMar 30, 2026OtherMW5186067
- KMEDIC LAMBOTTE OSTEOTOMEMar 30, 2026InjuryMW5186078
- ARTERIAL CATHETERIZATION KITMar 26, 2026MalfunctionMW5185983
- ARROW RADIAL ARTERIAL CATHETERIZATION SETJan 22, 2026InjuryMW5182638
- CHEST TUBE SYSTEMAug 28, 2025MalfunctionMW5175376
- ARROWG+ARD BLUE MAC TWO LUMEN CENTRAL VENOUS ACCESS FOR USE WITH 7.5-8May 20, 2025MalfunctionMW5170605
- ARROW PRESSURE INJECTABLE ARROWG+ARD BLUE PLUS THREE-LUMEN CVCAug 1, 2024MalfunctionMW5157929
- UROLIFTMay 23, 2024InjuryMW5155362
Recalls
0 on file
No recalls on file for this firm name.
Compliance history
Matched by FEI 3010041511.
FDA inspections
2 on file
- No Action Indicated (NAI)Mar 18, 2024
Compliance: Devices
- No Action Indicated (NAI)Mar 18, 2024
Compliance: Devices
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.