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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 28 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Mallinckrodt | 85865 | FDA UDI | Class I | Active |
| PowerCross | AB18W020040150 | FDA UDI | Class II | Active |
| Novafil | SPB-5833G | FDA UDI | Class II | Active |
| ClosureFast | MIS-7F07 | FDA UDI | Class II | Active |
| Endoflip | EF-301 | FDA UDI | Class II | Active |
| VersaOne | B12LGS | FDA UDI | Class II | Active |
| Shiley | 76260 | FDA UDI | Class II | Active |
| RapidVac | SEA3720 | FDA UDI | Class II | Active |
| Maxon | 8886 6267-51 | FDA UDI | Class II | Active |
| Chromic Gut | CG-904 | FDA UDI | Class II | Active |
| Polysorb | CL-913 | FDA UDI | Class II | Active |
| Caprosyn | SC-543 | FDA UDI | Class II | Active |
| Maxon | 8886 6311-63 | FDA UDI | Class II | Active |
| Protege GPS | SERB65-10-30-120 | FDA UDI | Class II | Active |
| Sonicision | SCBA | FDA UDI | U | Active |
| Mallinckrodt | 86207 | FDA UDI | Class II | Unknown |
| Monosof | SN-1792 | FDA UDI | Class II | Unknown |
| Syneture | US1664 | FDA UDI | Class II | Unknown |
| Visi-Pro™ | PXB35-06-57-080 | FDA UDI | Class II | Active |
| Auto Suture | OMS-T10BTNL | FDA UDI | Class II | Active |
| Endo GIA | EGIATRS45AXT | FDA UDI | Class II | Active |
| EverFlex | PRB35-06-060-080 | FDA UDI | Class III | Active |
| Mini Step | MS101008 | FDA UDI | Class II | Active |
| Edge | SDSEWCTE-FT | FDA UDI | Class II | Active |
| Situate | 01-0043V02-RFB | FDA UDI | Class I | Active |
| EverCross | AB35W05120080 | FDA UDI | Class II | Active |
| Visi-Pro | PXB35-08-57-135 | FDA UDI | Class II | Active |
| Shiley | M5.5PDC | FDA UDI | Class II | Active |
| Caprosyn | CC-813 | FDA UDI | Class II | Active |
| Protege GPS | SERB65-07-40-120 | FDA UDI | Class II | Active |
| Surgipro ll | VP-718-MX | FDA UDI | Class II | Unknown |
| Maxon | 8886621721-2 | FDA UDI | Class II | Active |
| Eea | TRIEEAXL21XTORVIL | FDA UDI | Class II | Active |
| Shiley | 96365 | FDA UDI | Class II | Active |
| Ti-Cron | 88862644-51 | FDA UDI | Class II | Unknown |
| Biosyn | CM-817 | FDA UDI | Class II | Active |
| RapidCross™ | A14BX020020170 | FDA UDI | Class II | Active |
| Endo GIA | 030426 | FDA UDI | Class II | Active |
| VersaOne | NONB11STF | FDA UDI | Class II | Active |
| Novafil | 8886 4403-43 | FDA UDI | Class II | Active |
| Puritan Bennett | 980IESYNC | FDA UDI | Class II | Active |
| Ti-Cron | 88862808-51 | FDA UDI | Class II | Active |
| Maxon | GMM-496L | FDA UDI | Class II | Active |
| PTFE Polymer Pledgets | 88868675-01 | FDA UDI | Class II | Active |
| Mallinckrodt | 86229 | FDA UDI | Class II | Active |
| Valleylab LS10 | VLLS10GEN | FDA UDI | Class II | Unknown |
| Eea | TRIEEAXL25MTORVIL | FDA UDI | Class II | Active |
| Surgipro II | VP702MX-2 | FDA UDI | Class II | Active |
| Monosof | N-2531 | FDA UDI | Class II | Active |
| Shiley | M3.5NEO | FDA UDI | Class II | Active |
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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. |