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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 7 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Polysorb | SL-5679G | FDA UDI | Class II | Active |
| Ti-Cron | 88863381-09 | FDA UDI | Class II | Active |
| Mallinckrodt | 18865 | FDA UDI | Class II | Active |
| Dar | 352U5877 | FDA UDI | Class II | Active |
| Nellcor | MAXALR | FDA UDI | Class II | Active |
| Fortrex | A35HPV07100040 | FDA UDI | Class II | Active |
| Fortrex | A35HPV09080080 | FDA UDI | Class II | Active |
| Chromic Gut | G-1792K | FDA UDI | Class II | Active |
| Dar | 444SP03014 | FDA UDI | Class I | Active |
| Sofsilk | VS889-2 | FDA UDI | Class II | Active |
| Mon-a-Therm | 90045 | FDA UDI | Class II | Active |
| Ti-Cron | 88862775-31 | FDA UDI | Class II | Active |
| Monosof | SN-764 | FDA UDI | Class II | Active |
| Polysorb | CLT-21-MG | FDA UDI | Class II | Active |
| Polysorb | CL-534 | FDA UDI | Class II | Active |
| RapidCross™ | A14BX040020090 | FDA UDI | Class II | Active |
| Shiley | 86451 | FDA UDI | Class II | Active |
| Puritan Bennett | 980U3FRDICU | FDA UDI | Class II | Unknown |
| Ti-Cron | XX-5165 | FDA UDI | Class II | Unknown |
| Ti-Cron | 88863336-51 | FDA UDI | Class II | Active |
| Polysorb | CL-904 | FDA UDI | Class II | Active |
| Nellcor | 10083058-RFB | FDA UDI | Class II | Unknown |
| Mini Step | MS101005 | FDA UDI | Class II | Active |
| Velosorb Fast | SVP-2251 | FDA UDI | Class II | Active |
| Protege GPS | SERB65-14-80-80 | FDA UDI | Class II | Active |
| Nitrex | N180603 | FDA UDI | Class II | Active |
| EverFlex™ | EVD35-06-080-150 | FDA UDI | Class III | Active |
| Surgipro ll | VP-721-MX | FDA UDI | Class II | Active |
| Fortrex | A35HPV12040135 | FDA UDI | Class II | Active |
| Polysorb | 170073 | FDA UDI | Class II | Active |
| Versaport Plus | NB8STF | FDA UDI | Class II | Unknown |
| Novafil | 8886 4410-03 | FDA UDI | Class II | Active |
| Emprint | CA30L1 | FDA UDI | Class II | Unknown |
| Syneture | VLOCL2246 | FDA UDI | Class II | Active |
| Chromic Gut | SG5687GMDL | FDA UDI | Class II | Unknown |
| Puritan Bennett | 980U1ESDIUA | FDA UDI | Class II | Active |
| TurboHawk™ | THS-LX-C | FDA UDI | Class II | Active |
| SilverHawk | P4055 | FDA UDI | Class II | Active |
| EverFlex™ | EVD35-08-020-150 | FDA UDI | Class III | Active |
| EverFlex™ | EVD35-08-020-080 | FDA UDI | Class III | Active |
| Shiley | M4.0PED | FDA UDI | Class II | Active |
| Biosyn | X-1294 | FDA UDI | Class II | Active |
| Dar | 444SP02414 | FDA UDI | Class I | Active |
| Shiley | M4SCT | FDA UDI | Class II | Active |
| Visi-Pro | PXB35-07-57-135 | FDA UDI | Class II | Active |
| Sonicision | SCDA13 | FDA UDI | U | Active |
| Edge | SD180EWCTE-FT | FDA UDI | Class II | Active |
| Puritan Bennett | 980U1ENDIUU-LA | FDA UDI | Class II | Unknown |
| Sofsilk | XX-5281 | FDA UDI | Class II | Active |
| Biosyn | UM-979 | FDA UDI | Class II | Unknown |
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. |