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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 4 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Surgipro II | SP5698GMDL | FDA UDI | Class II | Unknown |
| WarmTouch | 5030900 | FDA UDI | Class II | Active |
| Polysorb | CL-840 | FDA UDI | Class II | Active |
| Novafil | 8886 4452-41 | FDA UDI | Class II | Active |
| Fortrex™ | A35HPV04100040 | FDA UDI | Class II | Active |
| Novafil | XX2214 | FDA UDI | Class II | Unknown |
| Dar | 352/5901 | FDA UDI | Class II | Active |
| Valleylab | E250510FRNSB | FDA UDI | Class II | Active |
| Surgipro II | XX-5262 | FDA UDI | Class II | Unknown |
| Syneture | US1304 | FDA UDI | Class II | Unknown |
| Barrx | CYTO-KIT-R | FDA UDI | Class I | Active |
| Shiley | 86229 | FDA UDI | Class II | Active |
| Versaport Plus | NB11STS | FDA UDI | Class II | Unknown |
| Ti-Cron | X-1244 | FDA UDI | Class II | Unknown |
| Surgilon | 88861941-61 | FDA UDI | Class II | Unknown |
| RapidCross™ | A14BX040080170 | FDA UDI | Class II | Active |
| Shiley | M6LGT | FDA UDI | Class II | Active |
| Chromic Gut | SG-637 | FDA UDI | Class II | Active |
| Bis | 186-0224-NK | FDA UDI | Class II | Active |
| Surgilon | 88861920-62 | FDA UDI | Class II | Active |
| Ila | 3957 | FDA UDI | Class II | Unknown |
| Sofsilk | VS881-2 | FDA UDI | Class II | Active |
| Vascufil | 8886471011V-2 | FDA UDI | Class II | Active |
| VersaOne | UNVCA5LGF | FDA UDI | Class II | Active |
| Shiley | 2.5PEF | FDA UDI | Class II | Active |
| Surgipro ll | VP-904-MX | FDA UDI | Class II | Active |
| EverCross | AB35W12040135 | FDA UDI | Class II | Active |
| Shiley | 2.5PEF | FDA UDI | Class II | Active |
| Shiley | 5.5PLC | FDA UDI | Class II | Active |
| Stratis | 8101SS | FDA UDI | Class II | Unknown |
| TaperGuard | 18765S | FDA UDI | Class II | Active |
| Mallinckrodt | 86351 | FDA UDI | Class II | Unknown |
| VersaOne | UNVCA5STF | FDA UDI | Class II | Active |
| Arcpoint | ILS-2100-PN | FDA UDI | Class II | Active |
| Puritan Bennett | Y-103075-00A | FDA UDI | Class II | Unknown |
| Polysorb | SL-721 | FDA UDI | Class II | Active |
| Ti-Cron | XX-5175 | FDA UDI | Class II | Unknown |
| Polysorb | SL-1657 | FDA UDI | Class II | Active |
| Surgipro II | SP-8656G | FDA UDI | Class II | Unknown |
| Puritan Bennett | 980X1TRDRAC | FDA UDI | Class II | Active |
| Shiley | 33750 | FDA UDI | Class I | Unknown |
| RapidVac | SEA3741 | FDA UDI | Class II | Active |
| Fortrex | A35HPV10040040 | FDA UDI | Class II | Active |
| Maxon | 8886 6257-41 | FDA UDI | Class II | Active |
| Polysorb | GL-127 | FDA UDI | Class II | Active |
| Steel | 88862224-89 | FDA UDI | Class II | Active |
| Appose ULC | 8886803512 | FDA UDI | Class I | Active |
| Edge | SD301BAPK | FDA UDI | Class II | Active |
| ClosureFast | CB-CO-6 x 5 | FDA UDI | Class I | Unknown |
| superDimension | AED00147-20 | 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. |