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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 30 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| SilverHawk™ | P4056 | FDA UDI | Class II | Active |
| Visi-Pro™ | PXB35-05-17-080 | FDA UDI | Class III | Active |
| Nellcor | FLEXMAX-HC | FDA UDI | Class II | Active |
| RapidVac | SE3690 | FDA UDI | Class II | Active |
| Polysorb | CL-369-MG | FDA UDI | Class II | Active |
| RapidCross | A14BX020060170 | FDA UDI | Class II | Active |
| Shiley | 125237 | FDA UDI | Class II | Active |
| Biosyn | SM5637GMDL | FDA UDI | Class II | Unknown |
| Ti-Cron | X-1282 | FDA UDI | Class II | Unknown |
| Shiley | 8FEN | FDA UDI | Class II | Active |
| EverFlex | PRB35-07-100-080 | FDA UDI | Class III | Active |
| Steel | 88862413-83 | FDA UDI | Class II | Active |
| Polysorb | CL-15-MG | FDA UDI | Class II | Active |
| Shiley | 76270 | FDA UDI | Class II | Active |
| Surgilon | 88861883-51 | FDA UDI | Class II | Active |
| HawkOne™ | H1-S | FDA UDI | Class II | Active |
| Dar | 444SP03314 | FDA UDI | Class I | Active |
| RapidCross | A14BX035020170 | FDA UDI | Class II | Active |
| Polysorb | 170090 | FDA UDI | Class II | Active |
| Syneture | US1717 | FDA UDI | Class II | Unknown |
| V-Loc | VLOCN0326 | FDA UDI | Class II | Active |
| Dar | 444S02606 | FDA UDI | Class I | Active |
| McGRATH MAC | 350-017-000 | FDA UDI | Class I | Active |
| Dar | 444SPA2012 | FDA UDI | Class I | Active |
| Shiley | M5.0PED | FDA UDI | Class II | Active |
| Shiley | 86231 | FDA UDI | Class II | Unknown |
| Surgilon | CBST-851-MG | FDA UDI | Class II | Unknown |
| Surgipro II | SP-8619G | FDA UDI | Class II | Unknown |
| Ti-Cron | 88863050-51 | FDA UDI | Class II | Active |
| Step | S100000 | FDA UDI | Class II | Active |
| Invos | 5100C-PA | FDA UDI | Class II | Active |
| Polysorb | SL-822 | FDA UDI | Class II | Active |
| Auto Suture | OMST12BTNL | FDA UDI | Class II | Active |
| Mon-a-Therm | 502-0411A | FDA UDI | Class II | Active |
| Syneture | US1161 | FDA UDI | Class II | Unknown |
| Velosorb Fast | SV-834G | FDA UDI | Class II | Active |
| Ti-Cron | 88863003-52 | FDA UDI | Class II | Active |
| Shiley | 6CN75ES | FDA UDI | Class II | Unknown |
| Syneture | US1728 | FDA UDI | Class II | Unknown |
| LigaSure | LF3225 | FDA UDI | Class II | Active |
| Chromic Gut | CG-813 | FDA UDI | Class II | Active |
| Mallinckrodt | 86012 | FDA UDI | Class II | Active |
| EverFlex | PRB35-06-100-120 | FDA UDI | Class III | Active |
| Mallinckrodt | 86013 | FDA UDI | Class II | Active |
| Edge | SDMEWCTE-FT | FDA UDI | Class II | Active |
| Valtrac | 8886809100 | FDA UDI | Class II | Unknown |
| Caprosyn | SC-3639G | FDA UDI | Class II | Unknown |
| Edge | E1465-4 | FDA UDI | Class II | Active |
| Sofsilk | GS-64-M | FDA UDI | Class II | Active |
| Mild Chromic Gut | G-3794K | 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. |