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Sign in to claim this brandCovidien LP
US
Last updated May 24, 2026
Information
- Country
- US
- Address
- —
- Website
- covidien.com
- —
- —
- [email protected]
- Phone
- +1(508)261-8000
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 058614483
Catalogue (9686)
Page 29 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Evident | VTGEN | FDA UDI | Class II | Active |
| Maxon | 8886 6285-61 | FDA UDI | Class II | Active |
| Polysorb | CL-470 | FDA UDI | Class II | Unknown |
| HawkOne™ | H1-14550 | FDA UDI | Class II | Active |
| RapidCross | A14BX030060170 | FDA UDI | Class II | Active |
| Mon-a-Therm | 90054 | FDA UDI | Class II | Active |
| Fred 2 | 220-50 | FDA UDI | Class II | Active |
| Sofsilk | SS-787 | FDA UDI | Class II | Active |
| Step | S100712 | FDA UDI | Class II | Active |
| Ti-Cron | CDC-800 | FDA UDI | Class II | Unknown |
| Shiley | 87465 | FDA UDI | Class II | Active |
| Sofsilk | SS-673 | FDA UDI | Class II | Active |
| EverFlex™ | EVD35-08-100-080 | FDA UDI | Class III | Active |
| Invos | PMSENS71-A | FDA UDI | Class II | Active |
| Sofsilk | S-1734K | FDA UDI | Class II | Active |
| RapidCross™ | A14BX020060170 | FDA UDI | Class II | Active |
| Nitrex | N351803 | FDA UDI | Class II | Active |
| Protege RX Tapered | SECX-10-7-30-135 | FDA UDI | Class III | Active |
| Extended Tip Applicator | 205108 | FDA UDI | Class II | Unknown |
| Dar | 444SP01514 | FDA UDI | Class I | Active |
| Polysorb | SL-713 | FDA UDI | Class II | Unknown |
| WarmTouch | 5016000-RFB | FDA UDI | Class II | Active |
| Surgilon | X-1302 | FDA UDI | Class II | Active |
| Ti-Cron | 88863084-46 | FDA UDI | Class II | Active |
| Surgipro II | VP-417-X | FDA UDI | Class II | Unknown |
| Fortrex™ | A35HPV09080080 | FDA UDI | Class II | Active |
| Novafil | 88864538-63 | FDA UDI | Class II | Active |
| Nellcor | PM100N | FDA UDI | Class II | Active |
| Caprosyn | X-1353 | FDA UDI | Class II | Active |
| Polysorb | CL-819 | FDA UDI | Class II | Unknown |
| Visi-Pro™ | PXB35-06-17-080 | FDA UDI | Class III | Active |
| Shiley | 5-18541 | FDA UDI | Class II | Active |
| Mallinckrodt | 125041 | FDA UDI | Class II | Active |
| VersaOne | OBTONB12ST | FDA UDI | Class II | Active |
| Barrx | 90-9100 | FDA UDI | Class II | Active |
| TrailBlazer™Angled | ASC-035-150 | FDA UDI | Class II | Unknown |
| Sils | SILSHOOK36 | FDA UDI | Class II | Active |
| Biosyn | CMT-974 | FDA UDI | Class II | Active |
| Steel | 88862226-89 | FDA UDI | Class II | Active |
| EverFlex™ | EVD35-07-120-120 | FDA UDI | Class III | Active |
| Dar | 351S19044 | FDA UDI | Class II | Active |
| TurboHawk | THS-LS-C | FDA UDI | Class II | Active |
| RapidCross | A14BX040040170 | FDA UDI | Class II | Active |
| Polysorb | CL-545 | FDA UDI | Class II | Active |
| AqWire | A351801 | FDA UDI | Class II | Active |
| Puritan Bennett | 980S1PTDIUNA | FDA UDI | Class II | Active |
| Shiley | 86402 | FDA UDI | Class II | Active |
| Tri-Staple 2.0 | SIGCIR28MT | FDA UDI | Class II | Active |
| Puritan Bennett | 980X3NLDRAC | FDA UDI | Class II | Active |
| Polysorb | CL-544 | FDA UDI | Class II | Active |
Related Companies
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FDA Recalls (5)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Jul 17, 2017 | Z-0534-2018 | — | terminated | Medtronic is voluntarily recalling two production lots of its Covidien Vistec" x-ray detectable sponges de to possible contamination with human blood caused by handling of the product during the manufacturing process and prior to final packaging and Ethylene Oxide sterilization. |
| Dec 8, 2010 | Z-0954-2011 | — | terminated | During surgical procedures, the device may energize when clamping without pushing the activation button, which could result in unintended energy delivery to tissue. |
| Apr 21, 2006 | Z-0859-06 | — | terminated | Electrosurgical ablation device may experience loss of power during use, when used with Cool-tip Switching controller in ablation mode. |
| Jan 27, 2006 | Z-0772-06 | — | terminated | Sealing cycle may be interrupted during vessel ligation procedure, resulting in an incomplete seal. |
| Jan 27, 2006 | Z-0773-06 | — | terminated | Sealing cycle may be interrupted during vessel ligation procedure, resulting in an incomplete seal. |