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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 15 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Syneture | US1648 | FDA UDI | Class II | Unknown |
| Mallinckrodt | 76275 | FDA UDI | Class II | Active |
| Polysorb | SL-690 | FDA UDI | Class II | Active |
| Maxon | GMMT-761 | FDA UDI | Class II | Unknown |
| Novafil | XNF-1955 | FDA UDI | Class II | Unknown |
| Shiley | M4.0 PED | FDA UDI | Class II | Unknown |
| Mini Step | MS101003 | FDA UDI | Class II | Active |
| Shiley | 7CN80ED | FDA UDI | Class II | Active |
| Biosyn | UM-203 | FDA UDI | Class II | Active |
| Surgipro II | XX-5187 | FDA UDI | Class II | Unknown |
| Chromic Gut | UG-256 | FDA UDI | Class II | Unknown |
| TurboHawk™ | THS-SX-C | FDA UDI | Class II | Active |
| RapidCross™ | A14BX040060090 | FDA UDI | Class II | Active |
| Sofsilk | SS-734 | FDA UDI | Class II | Active |
| VersaStep | 177812 | FDA UDI | Class II | Unknown |
| Dar | 444S02805 | FDA UDI | Class I | Active |
| Mallinckrodt | 86402 | FDA UDI | Class II | Active |
| Valtrac | 8886808900 | FDA UDI | Class II | Unknown |
| Syneture | US1443 | FDA UDI | Class II | Unknown |
| Ti-Cron | 88863191-51 | FDA UDI | Class II | Active |
| Ila | 3971 | FDA UDI | Class II | Unknown |
| Biosyn | GMJ-62-M | FDA UDI | Class II | Active |
| Ti-Cron | X-1315 | FDA UDI | Class II | Unknown |
| Edge | E1551XNSB | FDA UDI | Class II | Active |
| Polysorb | L-28 | FDA UDI | Class II | Active |
| Ti-Cron | 88863260-52 | FDA UDI | Class II | Active |
| Vascufil | 88864722-21V | FDA UDI | Class II | Unknown |
| EverFlex™ | EVD35-06-020-150 | FDA UDI | Class III | Active |
| Nitrex | N352604 | FDA UDI | Class II | Active |
| Valleylab | E0020V | FDA UDI | Class II | Active |
| Ti-Cron | 88863218-56 | FDA UDI | Class II | Active |
| Syneture | US1469 | FDA UDI | Class II | Unknown |
| Ti-Cron | XX-5226 | FDA UDI | Class II | Active |
| Polysorb | SL-5628 | FDA UDI | Class II | Active |
| Syneture | US1624 | FDA UDI | Class II | Unknown |
| Chemosite | 120024 | FDA UDI | Class II | Unknown |
| Sofsilk | VS-622 | FDA UDI | Class II | Unknown |
| Puritan Bennett | 4-840220AIQC-FR | FDA UDI | Class II | Unknown |
| V-Loc 180 | VLOCL0305 | FDA UDI | Class II | Active |
| Polysorb | CL-871-L | FDA UDI | Class II | Active |
| Monosof | X-1317 | FDA UDI | Class II | Active |
| Fortrex | A35HPV05040135 | FDA UDI | Class II | Active |
| Ti-Cron | XX-5178 | FDA UDI | Class II | Unknown |
| Valleylab | E4060-CT | FDA UDI | Class II | Active |
| V-Loc 180 | VLOCL0223 | FDA UDI | Class II | Active |
| Valtrac | 8886809200 | FDA UDI | Class II | Unknown |
| Shiley | 86463 | FDA UDI | Class II | Unknown |
| Monosof | SN-5691G | FDA UDI | Class II | Unknown |
| Nellcor | MAXA-NS | FDA UDI | Class II | Active |
| Dar | 444SP00514 | FDA UDI | Class I | Active |
Related Companies
Authorised Representatives
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Importers
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Notified Bodies
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Authorities
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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. |