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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 9 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Surgiwip | ELW-43 | FDA UDI | Class II | Unknown |
| Mallinckrodt | 86209 | FDA UDI | Class II | Active |
| Biosyn | SM5687GMDL | FDA UDI | Class II | Unknown |
| PowerCross | AB18W040020150 | FDA UDI | Class II | Active |
| Nellcor | MAXN-NS | FDA UDI | Class II | Active |
| VersaOne | ONB12STF | FDA UDI | Class II | Active |
| Multifire VersaTack | 174021 | FDA UDI | Class II | Active |
| Fortrex | A35HPV07100080 | FDA UDI | Class II | Active |
| EverCross | AB35W06020135 | FDA UDI | Class II | Active |
| Shiley | 18710 | FDA UDI | Class II | Active |
| Polysorb | LL-115 | FDA UDI | Class II | Active |
| Wholey™ | WWIJ35145 | FDA UDI | Class II | Active |
| Nellcor | DLPM1000N-RR | FDA UDI | Class II | Unknown |
| Nellcor | DSPM10N-W | FDA UDI | Class II | Unknown |
| Surgipro ll | VP-901-MX | FDA UDI | Class II | Active |
| TurboHawk™ | THS-LS-C | FDA UDI | Class II | Active |
| Surgipro II | VP-762-X | FDA UDI | Class II | Active |
| RapidCross™ | A14BX040210090 | FDA UDI | Class II | Active |
| Dar | 5093500 | FDA UDI | Class II | Active |
| Ti-Cron | 8886264051-2 | FDA UDI | Class II | Unknown |
| Shiley | 85588 | FDA UDI | Class II | Unknown |
| Dar | 351S19044TC | FDA UDI | Class II | Active |
| IntraStent LD Max | S18-36 | FDA UDI | Class II | Active |
| Sofsilk | SS-695 | FDA UDI | Class II | Active |
| Nellcor | DLPM10N | FDA UDI | Class II | Active |
| Puritan Bennett | 4-076329-00 | FDA UDI | Class II | Unknown |
| Polysorb | SL-722 | FDA UDI | Class II | Active |
| PowerCross | AB18W060080150 | FDA UDI | Class II | Active |
| EverCross | AB35W05040135 | FDA UDI | Class II | Active |
| Polysorb | SL-5626G | FDA UDI | Class II | Unknown |
| Edge | E1465 | FDA UDI | Class II | Active |
| Polysorb | CL-602 | FDA UDI | Class II | Active |
| Shiley | 5.5PEF | FDA UDI | Class II | Active |
| Surgilon | 88861962-52 | FDA UDI | Class II | Active |
| Premium Polysorb | 013501L | FDA UDI | Class II | Unknown |
| Puritan Bennett | DF301 | FDA UDI | Class II | Unknown |
| Ti-Cron | 88863236-56 | FDA UDI | Class II | Active |
| Polysorb | L-33 | FDA UDI | Class II | Active |
| Puritan Bennett | 980NEOFLT | FDA UDI | Class II | Active |
| Ti-Cron | X-1146 | FDA UDI | Class II | Active |
| Ti-Cron | 88863336-41 | FDA UDI | Class II | Active |
| Polysorb | L-2749K | FDA UDI | Class II | Active |
| Shiley | M5.5 PED | FDA UDI | Class II | Unknown |
| Surgipro II | VP871XG | FDA UDI | Class II | Active |
| Monosof | SN-770G | FDA UDI | Class II | Active |
| Monosof | CN-824-L | FDA UDI | Class II | Unknown |
| Polysorb | CL-374-MG | FDA UDI | Class II | Active |
| Polysorb | L-1551-K | FDA UDI | Class II | Unknown |
| Shiley | SSVO | FDA UDI | Class II | Active |
| Nellcor | 902-I | 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. |