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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 21 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Valleylab | E2781-28 | FDA UDI | Class II | Active |
| Ti-Cron | 88862815-51 | FDA UDI | Class II | Active |
| RapidCross™ | A14BX035100090 | FDA UDI | Class II | Active |
| CleanCoat | E3772-36C | FDA UDI | Class II | Active |
| Dermalon | SDN-5933G | FDA UDI | Class II | Unknown |
| VersaOne | RNONB8LGF | FDA UDI | Class II | Active |
| Valleylab | E1562 | FDA UDI | Class II | Active |
| V-Loc 180 | VLOCL0615 | FDA UDI | Class II | Active |
| Spring Grip | 174104 | FDA UDI | Class II | Unknown |
| Polysorb | CL-260 | FDA UDI | Class II | Unknown |
| Syneture | US1675 | FDA UDI | Class II | Unknown |
| Monosof | SN-667 | FDA UDI | Class II | Active |
| Dar | 610U5257 | FDA UDI | Class I | Active |
| Dar | 444SP02314 | FDA UDI | Class I | Active |
| Shiley | 86125 | FDA UDI | Class II | Active |
| Monosof | CN830GL | FDA UDI | Class II | Unknown |
| Novafil | 8886 4002-41 | FDA UDI | Class II | Active |
| EverFlex™ | EVD35-06-020-120 | FDA UDI | Class III | Active |
| Novafil | 8886 4460-63 | FDA UDI | Class II | Active |
| Surgipro | SP-1697 | FDA UDI | Class II | Active |
| Cool-tip | SWCT1530 | FDA UDI | Class II | Active |
| Maxon | 8886 6751-61 | FDA UDI | Class II | Unknown |
| Maxon | 8886 6315-72 | FDA UDI | Class II | Unknown |
| EverCross | AB35W10020135 | FDA UDI | Class II | Active |
| Surgipro II | VP584X-2 | FDA UDI | Class II | Active |
| Novafil | 8886 4436-71 | FDA UDI | Class II | Active |
| Ti-Cron | 88863182-41 | FDA UDI | Class II | Active |
| Polysorb | CL-914 | FDA UDI | Class II | Active |
| Ti-Cron | 88862775-41 | FDA UDI | Class II | Active |
| Edge | E1452 | FDA UDI | Class II | Active |
| Spacemaker Plus | SMSBTOVL | FDA UDI | Class II | Active |
| Protege GPS | SERB65-07-80-120 | FDA UDI | Class II | Active |
| Dar | 444SP02010 | FDA UDI | Class I | Active |
| Shiley | 96585 | FDA UDI | Class II | Unknown |
| Dar | 444SP00516 | FDA UDI | Class I | Active |
| Monosof | SN-5696G | FDA UDI | Class II | Active |
| Surgipro | CP-453 | FDA UDI | Class II | Active |
| Powered Multifire Endo GIA | 030316L | FDA UDI | Class II | Unknown |
| Endo GIA | 030419 | FDA UDI | Class II | Unknown |
| Shiley | M2PT | FDA UDI | Class II | Active |
| Caprosyn | XX-5225 | FDA UDI | Class II | Unknown |
| Ti-Cron | 88863205-61 | FDA UDI | Class II | Active |
| Ti-Cron | 88863290-56 | FDA UDI | Class II | Active |
| Monosof | SN3697GMDL | FDA UDI | Class II | Unknown |
| Ti-Cron | 88863370-41 | FDA UDI | Class II | Active |
| Polysorb | L-1756K | FDA UDI | Class II | Active |
| Invos | IS-S | FDA UDI | Class II | Unknown |
| Valleylab | E2583-28 | FDA UDI | Class II | Unknown |
| Syneture | US1465 | FDA UDI | Class II | Unknown |
| Amplatz Goose Neck | SK701 | 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. |