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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 11 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ti-Cron | 88863379-62 | FDA UDI | Class II | Active |
| Puritan Bennett | S-232101-00B | FDA UDI | Class I | Unknown |
| NanoCross™ | AB14W020020090 | FDA UDI | Class II | Unknown |
| Valleylab | E1650 | FDA UDI | Class II | Active |
| Velosorb Fast | CV-2003G | FDA UDI | Class II | Active |
| VersaOne | NONB12STF | FDA UDI | Class II | Active |
| Nitrex | N351451 | FDA UDI | Class II | Active |
| Valleylab | E4053-CT | FDA UDI | Class II | Active |
| V-Loc 90 | VLOCM0625 | FDA UDI | Class II | Active |
| Cool-tip | ACTC1025 | FDA UDI | Class II | Active |
| Surgipro | CP-16-M | FDA UDI | Class II | Active |
| Polysorb | LL-233 | FDA UDI | Class II | Active |
| Monosof | SN-569 | FDA UDI | Class II | Unknown |
| Monosof | SN663GMDL | FDA UDI | Class II | Unknown |
| Ti-Cron | 88863117-61 | FDA UDI | Class II | Active |
| Caprosyn | CC-914 | FDA UDI | Class II | Active |
| V-Loc 180 | VLOCL0123 | FDA UDI | Class II | Active |
| Auto Suture | 4016 | FDA UDI | Class II | Unknown |
| Chromic Gut | CG-933 | FDA UDI | Class II | Active |
| Ti-Cron | CD-3113K | FDA UDI | Class II | Active |
| Polysorb | CL-304 | FDA UDI | Class II | Active |
| Ligasure | LS3092 | FDA UDI | Class II | Active |
| EverCross | AB35W04100135 | FDA UDI | Class II | Active |
| Surgipro ll | VP-720-MX | FDA UDI | Class II | Active |
| PowerCross | AB18W040150090 | FDA UDI | Class II | Active |
| Valleylab | E7506 | FDA UDI | Class II | Active |
| V-Loc 90 | VLOCM1624 | FDA UDI | Class II | Active |
| Nellcor | 10093313 | FDA UDI | Class II | Active |
| TruClear | 7209807S | FDA UDI | Class II | Active |
| Dar | 331D5656 | FDA UDI | Class I | Active |
| RapidCross™ | A14BX035060090 | FDA UDI | Class II | Active |
| Maxon | CMM-582G | FDA UDI | Class II | Unknown |
| VersaOne | RC12LGS | FDA UDI | Class II | Active |
| Surgipro | SP-1664G | FDA UDI | Class II | Unknown |
| Syneture | US1722 | FDA UDI | Class II | Unknown |
| Surgipro II | VP972X | FDA UDI | Class II | Active |
| Mon-a-Therm | 90056 | FDA UDI | Class II | Active |
| Mallinckrodt | 18760 | FDA UDI | Class II | Active |
| Puritan Bennett | 980U3ENDIUU-LA | FDA UDI | Class II | Active |
| Puritan Bennett | 980X1DEDISS | FDA UDI | Class II | Active |
| Polysorb | CL-824-L | FDA UDI | Class II | Active |
| V-Loc 180 | VLOCL0644 | FDA UDI | Class II | Active |
| Polysorb | XX-5214 | FDA UDI | Class II | Unknown |
| Valleylab | E2783R-28ASP | FDA UDI | Class II | Unknown |
| Novafil | 8886 4458-63 | FDA UDI | Class II | Active |
| Emprint HP | CAGENHP | FDA UDI | Class II | Active |
| Syneture | VLOCN2145 | FDA UDI | Class II | Active |
| Surgipro II | VP-751-MX | FDA UDI | Class II | Unknown |
| Edge | SD300BA | FDA UDI | Class II | Active |
| Dar | 354/5841 | FDA UDI | Class I | 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. |