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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 33 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Caprosyn | LC-113 | FDA UDI | Class II | Unknown |
| Maxon | 8886 6534-21 | FDA UDI | Class II | Unknown |
| Endo Mini-Shears | 174301 | FDA UDI | Class II | Active |
| Caprosyn | CC-844 | FDA UDI | Class II | Active |
| Plain Gut | SG-604 | FDA UDI | Class II | Unknown |
| Bis | 186-0137 | FDA UDI | Class II | Active |
| RapidCross™ | A14BX020040090 | FDA UDI | Class II | Active |
| EverCross | AB35W03040135 | FDA UDI | Class II | Active |
| Fortrex | A35HPV05100080 | FDA UDI | Class II | Active |
| Ti-Cron | 8886264551-2 | FDA UDI | Class II | Unknown |
| Dar | 444SP02114 | FDA UDI | Class I | Active |
| Surgipro | SPMM-14 | FDA UDI | Class II | Unknown |
| Novafil | 8886 4420-43 | FDA UDI | Class II | Active |
| Valleylab | E1653 | FDA UDI | Class II | Active |
| Velosorb Fast | CV-417G | FDA UDI | Class II | Active |
| Valleylab | E3310NSB | FDA UDI | Class II | Active |
| Puritan Bennett | 980U3ESDIUC | FDA UDI | Class II | Unknown |
| Polysorb | CL-457 | FDA UDI | Class II | Active |
| Novafil | SPB-5413G | FDA UDI | Class II | Active |
| Mallinckrodt | 86011 | FDA UDI | Class II | Unknown |
| Dar | 444SP02014 | FDA UDI | Class I | Active |
| Barrx | 90-9500 | FDA UDI | Class II | Active |
| EverCross | AB35W12060080 | FDA UDI | Class II | Active |
| Puritan Bennett | 10086051 | FDA UDI | Class II | Active |
| Maxon | 8886 6219-43 | FDA UDI | Class II | Unknown |
| Sils | SILSCLINCH36 | FDA UDI | Class II | Unknown |
| ClosureFast | AN-19G | FDA UDI | Class I | Active |
| Fortrex™ | A35HPV05020080 | FDA UDI | Class II | Active |
| Vital Sync | Vital Sync v2.6 | FDA UDI | Class II | Active |
| Syneture | US1718 | FDA UDI | Class II | Active |
| Monosof | SN-660 | FDA UDI | Class II | Active |
| Shiley | M10FEN | FDA UDI | Class II | Active |
| Surgilon | 88861953-32J | FDA UDI | Class II | Active |
| TA Premium | 015441L | FDA UDI | Class II | Active |
| Puritan Bennett | 980X1ENDICU | FDA UDI | Class II | Unknown |
| Surgipro II | XX-5117 | FDA UDI | Class II | Active |
| Puritan Bennett | 4-840220DISS-EN | FDA UDI | Class II | Unknown |
| Valleylab | E2515HDA | FDA UDI | Class II | Active |
| Mallinckrodt | 86550 | FDA UDI | Class II | Active |
| V-Loc 180 | VLOCL2836 | FDA UDI | Class II | Active |
| V-Loc 90 | VLOCM1203 | FDA UDI | Class II | Active |
| Dar | 331/5385 | FDA UDI | Class I | Active |
| Ti-Cron | 88863054-51 | FDA UDI | Class II | Active |
| Polysorb | UL-670 | FDA UDI | Class II | Unknown |
| Maxon | 8886614921-2 | FDA UDI | Class II | Active |
| Polysorb | CL-201-M | FDA UDI | Class II | Active |
| Nitrex | N141802 | FDA UDI | Class II | Active |
| Syneture | US1474 | FDA UDI | Class II | Unknown |
| Surgipro | SP-690 | FDA UDI | Class II | Active |
| Mallinckrodt | 86656 | 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. |