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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 25 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Puritan Bennett | 4-840220NISC-FR | FDA UDI | Class II | Unknown |
| Steel | 88862224-69 | FDA UDI | Class II | Active |
| Polysorb | GLT-69-MG | FDA UDI | Class II | Active |
| Velosorb Fast | SV-2297 | FDA UDI | Class II | Active |
| Versaport | UNVCA12STF | FDA UDI | Class II | Active |
| Mild Chromic Gut | G-3898 | FDA UDI | Class II | Unknown |
| Monosof | CN-845 | FDA UDI | Class II | Unknown |
| Surgipro ll | SP-5687G | FDA UDI | Class II | Active |
| Biosyn | GM-64-M | FDA UDI | Class II | Unknown |
| Puritan Bennett | Y-100872-00 | FDA UDI | Class II | Unknown |
| Tri-Staple 2.0 | SIGCIR31MT | FDA UDI | Class II | Active |
| V-Loc 90 | VLOCM0134 | FDA UDI | Class II | Active |
| Biosyn | M-23 | FDA UDI | Class II | Active |
| Monosof | CN-290 | FDA UDI | Class II | Unknown |
| Fortrex | A35HPV08100135 | FDA UDI | Class II | Active |
| Velosorb Fast | SV-9937G | FDA UDI | Class II | Unknown |
| Ti-Cron | 88863218-36 | FDA UDI | Class II | Active |
| Ti-Cron | 88863160-51 | FDA UDI | Class II | Active |
| V-Loc 90 | VLOCM1704 | FDA UDI | Class II | Active |
| Caprosyn | CC-1945G | FDA UDI | Class II | Active |
| Het | 180-1007 | FDA UDI | Class II | Active |
| Shiley | 109870 | FDA UDI | Class II | Active |
| Puritan Bennett | 4-076325-00 | FDA UDI | Class II | Active |
| V-Loc 90 | VLOCM0316 | FDA UDI | Class II | Active |
| VersaOne | B12STFCS | FDA UDI | Class II | Active |
| Endo GIA | 030455 | FDA UDI | Class II | Active |
| Polysorb | CL-517 | FDA UDI | Class II | Active |
| Shiley | 80XLTUP | FDA UDI | Class II | Active |
| Fortrex | A35HPV12040080 | FDA UDI | Class II | Active |
| Force Triverse | FT3000DB | FDA UDI | Class II | Active |
| Caprosyn | SC-5690G | FDA UDI | Class II | Active |
| Shiley | 86288 | FDA UDI | Class II | Active |
| Dermalon | 88861756-31 | FDA UDI | Class II | Active |
| Maxon | SMM-5221 | FDA UDI | Class II | Active |
| Ti-Cron | XX-5077 | FDA UDI | Class II | Unknown |
| Ti-Cron | 88863277-56 | FDA UDI | Class II | Active |
| Polysorb | CLS-954 | FDA UDI | Class II | Unknown |
| Syneture | US1720 | FDA UDI | Class II | Unknown |
| Mallinckrodt | 86398 | FDA UDI | Class II | Active |
| Surgipro ll | VP-712-MX | FDA UDI | Class II | Active |
| Dar | 332/5317 | FDA UDI | Class I | Active |
| Fortrex | A35HPV07080135 | FDA UDI | Class II | Active |
| Shiley | M3.0NEO | FDA UDI | Class II | Active |
| Polysorb | LL-113 | FDA UDI | Class II | Active |
| Surgipro II | VP-751-X | FDA UDI | Class II | Active |
| Syneture | US1575 | FDA UDI | Class II | Unknown |
| Mallinckrodt | 86201 | FDA UDI | Class II | Active |
| Biosyn | CMT-740-M | FDA UDI | Class II | Active |
| Kendall | 1181200555K | FDA UDI | Class II | Active |
| Protege EverFlex | PRB35-05-080-080 | FDA UDI | Class II | Active |
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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. |