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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 16 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Mallinckrodt | 126037 | FDA UDI | Class II | Active |
| Polysorb | L-101 | FDA UDI | Class II | Unknown |
| Syneture | US0286 | FDA UDI | Class II | Unknown |
| Polysorb | SL-5648 | FDA UDI | Class II | Unknown |
| Sm | 050284 | FDA UDI | Class I | Unknown |
| Polysorb | SL-652G | FDA UDI | Class II | Unknown |
| Mallinckrodt | 86646 | FDA UDI | Class II | Active |
| Syneture | US1041 | FDA UDI | Class II | Unknown |
| Surgipro ll | VPF-710-X | FDA UDI | Class II | Active |
| Polysorb | L-113 | FDA UDI | Class II | Active |
| RapidCross | A14BX035100090 | FDA UDI | Class II | Active |
| Surgipro ll | VPF-726-X | FDA UDI | Class II | Active |
| Surgidac | XX-5012 | FDA UDI | Class II | Unknown |
| Syneture | US1274T | FDA UDI | Class II | Unknown |
| RapidCross™ | A14BX025150170 | FDA UDI | Class II | Active |
| Dar | 350/5879 | FDA UDI | Class II | Active |
| Shiley | 125141 | FDA UDI | Class II | Active |
| Situate | L1818-04P01CN-L | FDA UDI | Class I | Active |
| Shiley | M2.5PT | FDA UDI | Class II | Active |
| Sofsilk | GS452-2 | FDA UDI | Class II | Active |
| RapidCross | A14BX025120170 | FDA UDI | Class II | Active |
| Dar | 351/5835 | FDA UDI | Class II | Active |
| Shiley | 125139 | FDA UDI | Class II | Active |
| Bis | 186-0199-PH | FDA UDI | Class II | Active |
| Polysorb | XX-5131 | FDA UDI | Class II | Unknown |
| Surgipro | VP-628 | FDA UDI | Class II | Active |
| Monosof | SN-867 | FDA UDI | Class II | Unknown |
| Surgipro II | SP5686GMDL | FDA UDI | Class II | Unknown |
| Biosyn | CM-776L | FDA UDI | Class II | Active |
| Maxon | SMM-5516 | FDA UDI | Class II | Active |
| V-Loc 90 | VLOCM0336 | FDA UDI | Class II | Active |
| Dermalon | 88861764-51 | FDA UDI | Class II | Active |
| Polysorb | CL-4M | FDA UDI | Class II | Active |
| Biosyn | CMT-952 | FDA UDI | Class II | Unknown |
| Polysorb | CL-843 | FDA UDI | Class II | Active |
| Protege EverFlex | PRB35-05-020-080 | FDA UDI | Class II | Active |
| Puritan Bennett | 980N3ESDIUC | FDA UDI | Class II | Unknown |
| Bis | 186-0106-PH | FDA UDI | Class II | Active |
| Puritan Bennett | 4-002536-00 | FDA UDI | Class I | Unknown |
| Eea | TRIEEAXL31MT | EUDAMEDFDA UDI | Class II | Active |
| Mallinckrodt | 125237 | FDA UDI | Class II | Active |
| EverCross | AB35W06030135 | FDA UDI | Class II | Active |
| Puritan Bennett | 10049984 | FDA UDI | Class II | Unknown |
| Surgilon | 88861964-61 | FDA UDI | Class II | Active |
| Syneture | US1666 | FDA UDI | Class II | Unknown |
| Polysorb | CL-839 | FDA UDI | Class II | Active |
| Velosorb Fast | CV-0046 | FDA UDI | Class II | Active |
| Biosyn | SM-5628 | FDA UDI | Class II | Active |
| Polysorb | CLT-260 | FDA UDI | Class II | Unknown |
| Caprosyn | SC-5626 | 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. |