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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 24 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| V-Loc 90 | VLOCM3225 | FDA UDI | Class II | Active |
| Polysorb | L-0213K | FDA UDI | Class II | Unknown |
| Caprosyn | SC-587 | FDA UDI | Class II | Active |
| RapidVac | SEA3745 | FDA UDI | Class II | Active |
| Surgilon | 88862011-51 | FDA UDI | Class II | Active |
| Polysorb | CL-950 | FDA UDI | Class II | Active |
| EverFlex™ | EVD35-06-020-080 | FDA UDI | Class III | Active |
| Shiley | 125128 | FDA UDI | Class II | Active |
| Maxon | XX-2109 | FDA UDI | Class II | Active |
| Puritan Bennett | 980X3DENISS | FDA UDI | Class II | Unknown |
| Surgilon | 88861914-73 | FDA UDI | Class II | Unknown |
| Mallinckrodt | 96222 | FDA UDI | Class II | Unknown |
| Caprosyn | XX-5245 | FDA UDI | Class II | Unknown |
| Edge | E1450-4 | FDA UDI | Class II | Active |
| Herculon | H0003 | FDA UDI | Class II | Unknown |
| Eea | EEATAID21D | FDA UDI | Class I | Unknown |
| Polysorb | SL-613 | FDA UDI | Class II | Active |
| PowerCross | AB18W030200150 | FDA UDI | Class II | Active |
| Sonicision | SCD391 | FDA UDI | U | Active |
| Biosyn | XX-5006 | FDA UDI | Class II | Unknown |
| Polysorb | CL-886-M | FDA UDI | Class II | Active |
| Polysorb | CL-52-MG | FDA UDI | Class II | Active |
| Shiley | M6LPC | FDA UDI | Class II | Active |
| Dar | 331/5668 | FDA UDI | Class I | Active |
| Dar | 351/5856 | FDA UDI | Class II | Active |
| V-Loc 90 | VLOCM3245 | FDA UDI | Class II | Active |
| Surgipro | CP-414 | FDA UDI | Class II | Active |
| Syneture | US1747 | FDA UDI | Class II | Unknown |
| Versaport | UNVCA11STF | FDA UDI | Class II | Active |
| Multifire Endo Hernia | 174015 | FDA UDI | Class II | Active |
| Surgipro II | VP-985-X | FDA UDI | Class II | Unknown |
| Shiley | 86285 | FDA UDI | Class II | Unknown |
| Ti-Cron | 88863376-81 | FDA UDI | Class II | Active |
| Mild Chromic Gut | G-3790K | FDA UDI | Class II | Active |
| Surgipro | CP-10-M | FDA UDI | Class II | Active |
| TaperGuard | 18775S | FDA UDI | Class II | Active |
| Surgipro ll | X-1148 | FDA UDI | Class II | Unknown |
| Polysorb | SL-171 | FDA UDI | Class II | Active |
| Monosof | N-2757K | FDA UDI | Class II | Active |
| RapidCross™ | A14BX030040170 | FDA UDI | Class II | Active |
| Wholey™ | WWFS35145 | FDA UDI | Class II | Active |
| Fortrex™ | A35HPV12040080 | FDA UDI | Class II | Active |
| Puritan Bennett | G-760110DIUU-JP | FDA UDI | Class II | Unknown |
| Syneture | US1625 | FDA UDI | Class II | Unknown |
| Surgipro II | XX-5259 | FDA UDI | Class II | Active |
| Monosof | GNJ-283 | FDA UDI | Class II | Active |
| Pi | 3926L | FDA UDI | Class II | Unknown |
| Fortrex™ | A35HPV08080080 | FDA UDI | Class II | Active |
| RapidCross | A14BX035060090 | FDA UDI | Class II | Active |
| Sofsilk | SS-629 | 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. |