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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 2 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Powered Multifire Endo GIA | 030306 | FDA UDI | Class II | Unknown |
| Puritan Bennett | 4-074647-00 | FDA UDI | Class II | Active |
| Biosyn | SM-822 | FDA UDI | Class II | Active |
| Polysorb | CL-850-M | FDA UDI | Class II | Unknown |
| Dar | 352/5805TC | FDA UDI | Class II | Active |
| RapidCross™ | A14BX040100170 | FDA UDI | Class II | Active |
| Puritan Bennett | 4-840220DIAC-EN | FDA UDI | Class II | Unknown |
| VersaStep | VS100705 | FDA UDI | Class II | Active |
| Lapro-Clip | 8886848813 | FDA UDI | Class II | Active |
| Mallinckrodt | 125241 | FDA UDI | Class II | Active |
| V-Loc 90 | VLOCM1824 | FDA UDI | Class II | Active |
| Surgipro | SP-868G | FDA UDI | Class II | Active |
| Dermalon | 88861771-43 | FDA UDI | Class II | Unknown |
| Syneture | US1751 | FDA UDI | Class II | Unknown |
| Evident | VT1220 | FDA UDI | Class II | Unknown |
| Situate | 01-0043 | FDA UDI | Class I | Active |
| Sofsilk | VS-880 | FDA UDI | Class II | Unknown |
| Situate | TOR-0101C-1 | FDA UDI | Class I | Active |
| Ti-Cron | 88863271-41 | FDA UDI | Class II | Active |
| Surgilon | X-1246 | FDA UDI | Class II | Unknown |
| Dar | 444SP02110 | FDA UDI | Class I | Active |
| TrailBlazer™ Angled | ASC-014-090 | FDA UDI | Class II | Active |
| V-Loc 90 | VLOCM2044 | FDA UDI | Class II | Active |
| Polysorb | L-2752K | FDA UDI | Class II | Active |
| Polysorb | GLS-323 | FDA UDI | Class II | Active |
| Wholey™ | WWSS35175 | FDA UDI | Class II | Active |
| Ti-Cron | X-1298 | FDA UDI | Class II | Unknown |
| Shiley | M6DCFN | FDA UDI | Class II | Active |
| Dar | 354/5920 | EUDAMEDFDA UDI | Class I | Active |
| Surgipro II | VP581X-2 | FDA UDI | Class II | Active |
| Surgilon | 88861998-62 | FDA UDI | Class II | Active |
| Situate | TORW-0101CN-1 | FDA UDI | Class I | Active |
| Shiley | M8LPC | FDA UDI | Class II | Active |
| Puritan Bennett | 980U3ESDIUA | FDA UDI | Class II | Unknown |
| SpiderFX | SPD2-US-030-190 | FDA UDI | Class II | Active |
| EverFlex | PRB35-06-150-120 | FDA UDI | Class III | Active |
| EverFlex™ | EVD35-06-120-120 | FDA UDI | Class III | Active |
| SurgiSleeve | WPLG914 | FDA UDI | Class II | Active |
| Novafil | 8886 4459-51 | FDA UDI | Class II | Active |
| Ti-Cron | X-1227 | FDA UDI | Class II | Unknown |
| Versaport Plus | 177994P | FDA UDI | Class II | Unknown |
| Polysorb | CL-045 | FDA UDI | Class II | Active |
| Mallinckrodt | 86007 | FDA UDI | Class II | Unknown |
| Syneture | US1254 | FDA UDI | Class II | Unknown |
| Shiley | 3.0NEF | FDA UDI | Class II | Active |
| Oridion | N85 | FDA UDI | Class II | Unknown |
| Shiley | 10FENJ | FDA UDI | Class II | Active |
| Puritan Bennett | 10051458 | FDA UDI | Class II | Unknown |
| Tri-Staple 2.0 | SIGRADXT | FDA UDI | Class II | Active |
| Puritan Bennett | 4-840220DIEP-EN | FDA UDI | Class II | Unknown |
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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. |