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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 8 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Shiley | 86455 | FDA UDI | Class II | Active |
| Dar | 332/5332 | FDA UDI | Class I | Active |
| Steel | 88862392-49 | FDA UDI | Class II | Active |
| RapidCross | A14BX030020170 | FDA UDI | Class II | Active |
| EverCross | AB35W04200080 | FDA UDI | Class II | Active |
| Nitrex | N183002 | FDA UDI | Class II | Active |
| Shiley | 125035 | FDA UDI | Class II | Active |
| Surgilon | 88861993-62 | FDA UDI | Class II | Active |
| Monosof | SN-662G | FDA UDI | Class II | Active |
| EverCross | AB35W06080040 | FDA UDI | Class II | Active |
| Maxon | 8886 6261-61 | FDA UDI | Class II | Active |
| Ti-Cron | 88862947-53 | FDA UDI | Class II | Active |
| Polysorb | CL-844 | FDA UDI | Class II | Active |
| Shiley | 125035 | FDA UDI | Class II | Active |
| Shiley | 86445 | FDA UDI | Class II | Active |
| Dar | 444SP02516 | FDA UDI | Class I | Active |
| Ti-Cron | VCD2036305FE | FDA UDI | Class II | Active |
| Chemosite | 120047 | FDA UDI | Class II | Unknown |
| Syneture | US1661 | FDA UDI | Class II | Unknown |
| Syneture | US1631 | FDA UDI | Class II | Unknown |
| Caprosyn | GC123G | FDA UDI | Class II | Unknown |
| Caprosyn | XX-5183 | FDA UDI | Class II | Unknown |
| Monosof | SN-775 | FDA UDI | Class II | Active |
| Surgilon | 88861909-62 | FDA UDI | Class II | Active |
| Polysorb | CL-814 | FDA UDI | Class II | Active |
| EverCross | AB35W08080080 | FDA UDI | Class II | Active |
| Maxon | XX-2121 | FDA UDI | Class II | Unknown |
| Dar | 444SPA2312 | FDA UDI | Class I | Active |
| Nellcor | AI | FDA UDI | Class II | Unknown |
| Ti-Cron | X-1176 | FDA UDI | Class II | Unknown |
| Polysorb | EL-410 | FDA UDI | Class II | Unknown |
| Shiley | M5.0PDC | FDA UDI | Class II | Active |
| iDrive | INTBIG | FDA UDI | Class II | Unknown |
| Chromic Gut | CG-922 | FDA UDI | Class II | Active |
| Stat Tack | OMS-TTSS | FDA UDI | Class II | Active |
| Velosorb Fast | SV-2295 | FDA UDI | Class II | Active |
| Puritan Bennett | 10086042 | FDA UDI | Class II | Active |
| Polysorb | CL-356-MG | FDA UDI | Class II | Active |
| Surgipro II | VP-75-X | FDA UDI | Class II | Active |
| V-Loc 180 | VLOCL0113 | FDA UDI | Class II | Unknown |
| PTFE Polymer Pledgets | 88868682-01 | FDA UDI | Class II | Active |
| Maxon CV | 8886 6124-11 | FDA UDI | Class II | Unknown |
| Endo GIA Ultra | EGIAUSTND | FDA UDI | Class II | Active |
| V-Loc 90 | VLOCM2116 | FDA UDI | Class II | Active |
| Versaport | ONB5SHF | FDA UDI | Class II | Active |
| V-Loc 90 | VLOCM0306 | FDA UDI | Class II | Active |
| EverFlex™ | EVD35-06-060-150 | FDA UDI | Class III | Active |
| V-Loc 90 | VLOCM0123 | FDA UDI | Class II | Active |
| Maxon | VMM-137 | FDA UDI | Class II | Unknown |
| Maxon CV | 8886 6127-11 | FDA UDI | Class II | Unknown |
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. |