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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 34 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Shiley | 5-18537 | FDA UDI | Class II | Active |
| Mallinckrodt | 125037 | FDA UDI | Class II | Active |
| Ti-Cron | 88863259-52 | FDA UDI | Class II | Active |
| Chromic Gut | CG-883 | FDA UDI | Class II | Active |
| SurgiStat | SURGII20ZD | FDA UDI | Class II | Active |
| VersaOne | RNONB12STF | FDA UDI | Class II | Unknown |
| Invos | PM7100 | FDA UDI | Class II | Active |
| V-Loc 180 | VLOCA206L | FDA UDI | Class II | Active |
| Mallinckrodt | 86204 | FDA UDI | Class II | Active |
| Valleylab | GR200A | FDA UDI | Class II | Active |
| Maxon | 8886 6235-31 | FDA UDI | Class II | Active |
| Endo Dissect | 174213 | FDA UDI | Class I | Active |
| V-Loc 180 | VLOCL0314 | FDA UDI | Class II | Unknown |
| Signia | SIGADAPTSTND | FDA UDI | Class II | Active |
| Edge | SD302BA | FDA UDI | Class II | Active |
| Syneture | US1673 | FDA UDI | Class II | Unknown |
| Ti-Cron | XX-5164 | FDA UDI | Class II | Unknown |
| McGRATH MAC | 350-072-000 | FDA UDI | Class I | Active |
| Polysorb | CL-382-MG | FDA UDI | Class II | Unknown |
| Polysorb | CL-055 | FDA UDI | Class II | Active |
| Ti-Cron | 88863258-42 | FDA UDI | Class II | Active |
| Puritan Bennett | 980X3ENDISS | FDA UDI | Class II | Active |
| Valleylab | E1550 | FDA UDI | Class II | Active |
| Ti-Cron | 88863048-51 | FDA UDI | Class II | Active |
| RapidCross™ | A14BX025100090 | FDA UDI | Class II | Active |
| Maxon | SMM-5033 | FDA UDI | Class II | Active |
| Mallinckrodt | 18770 | FDA UDI | Class II | Active |
| Syneture | US1685 | FDA UDI | Class II | Unknown |
| SilverHawkTM | P4030 | FDA UDI | Class II | Active |
| Surgipro II | X-1363 | FDA UDI | Class II | Unknown |
| Maxon | 8886 6626-51 | FDA UDI | Class II | Active |
| Endo GIA | EGIA60AVM | FDA UDI | Class II | Active |
| V-Loc 180 | VLOCL0625 | FDA UDI | Class II | Active |
| Biosyn | CM-31-M | FDA UDI | Class II | Active |
| Maxon CV | 8886 6132-11 | FDA UDI | Class II | Active |
| EverFlex™ | EVD35-08-040-080 | FDA UDI | Class III | Active |
| EverFlex | PRB35-08-030-120 | FDA UDI | Class III | Active |
| Protege GPS | SERB65-12-30-80 | FDA UDI | Class II | Active |
| Vital Sync | EWS v1.0 | FDA UDI | Class I | Active |
| EverFlex | EVD35-07200120 | FDA UDI | Class III | Active |
| EverCross | AB35W03060080 | FDA UDI | Class II | Active |
| Biosyn | UM-978 | FDA UDI | Class II | Active |
| Mallinckrodt | 125141 | FDA UDI | Class II | Active |
| Dar | 444SP01012 | FDA UDI | Class I | Active |
| Maxon | XX-2117 | FDA UDI | Class II | Unknown |
| Monosof | SN-662 | FDA UDI | Class II | Active |
| Shiley | 86236 | FDA UDI | Class II | Active |
| Visi-Pro™ | PXB35-06-12-080 | FDA UDI | Class II | Active |
| Endo GIA Ultra | EGIAUXL | FDA UDI | Class II | Active |
| Chromic Gut | CG-914 | 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. |