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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 23 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Maxon | 88866277-71 | FDA UDI | Class II | Unknown |
| Fortrex™ | A35HPV07080135 | FDA UDI | Class II | Active |
| Dar | R026 | FDA UDI | Class II | Active |
| Poly Surgiclip | 133649 | FDA UDI | Class II | Unknown |
| Ti-Cron | 88862978-51 | FDA UDI | Class II | Active |
| Maxon | 8886620731-2 | FDA UDI | Class II | Active |
| Shiley | 60XLTCD | FDA UDI | Class II | Active |
| Puritan Bennett | 10051472 | FDA UDI | Class II | Unknown |
| Gia | GIA60XTC | FDA UDI | Class II | Active |
| Tri-Staple 2.0 | SIGC60VT | FDA UDI | Class II | Active |
| Force EZ | Force EZ-C | FDA UDI | Class II | Active |
| Sofsilk | VS-810 | FDA UDI | Class II | Unknown |
| Shiley | M2.5PT | FDA UDI | Class II | Active |
| Shiley | 6IC75 | FDA UDI | Class II | Active |
| Puritan Bennett | 980X1DEDRAC | FDA UDI | Class II | Active |
| Velosorb Fast | CV-322 | FDA UDI | Class II | Active |
| Premium Multifire TA | 010315 | FDA UDI | Class I | Unknown |
| Puritan Bennett | S-231699-00B | FDA UDI | Class I | Unknown |
| AS Meniscal | 1001001SS | FDA UDI | Class II | Unknown |
| Surgipro | X-1209 | FDA UDI | Class II | Active |
| Ti-Cron | XX-5234 | FDA UDI | Class II | Active |
| Polysorb | GL-124 | FDA UDI | Class II | Active |
| Surgipro II | VP-542X | FDA UDI | Class II | Active |
| Shiley | 86268 | FDA UDI | Class II | Active |
| Mallinckrodt | 96365 | FDA UDI | Class II | Active |
| Dar | 444S02710 | FDA UDI | Class I | Active |
| Shiley | M5.5PED | FDA UDI | Class II | Active |
| Shiley | 5CN70ES | FDA UDI | Class II | Active |
| Syneture | US1299 | FDA UDI | Class II | Unknown |
| Maxon | SMM-5831 | FDA UDI | Class II | Active |
| LigaSure | LF1544 | FDA UDI | Class II | Active |
| Syneture | US1552 | FDA UDI | Class II | Unknown |
| Fortrex™ | A35HPV06100040 | FDA UDI | Class II | Active |
| Ti-Cron | X-1216 | FDA UDI | Class II | Active |
| Polysorb | CL-932 | FDA UDI | Class II | Active |
| Protege RX | SECX-10-30-135 | FDA UDI | Class III | Active |
| Syneture | US0981 | FDA UDI | Class II | Unknown |
| Tri-Staple 2.0 | SIGCIRIC | FDA UDI | Class II | Unknown |
| Valleylab | Force Argon II-20 | FDA UDI | Class II | Active |
| Velosorb Fast | SV-2930 | FDA UDI | Class II | Active |
| Surgipro | CP-434 | FDA UDI | Class II | Active |
| Tri-Staple 2.0 | SIGTRS45AXT | FDA UDI | Class II | Unknown |
| Valleylab | SEA50595 | FDA UDI | Class II | Active |
| Shiley | M10DCT | FDA UDI | Class II | Active |
| Surgipro II | VP720X-2 | FDA UDI | Class II | Active |
| Sofsilk | X-1101 | FDA UDI | Class II | Unknown |
| TaperGuard | 18710S | FDA UDI | Class II | Active |
| Sofsilk | CS-211 | FDA UDI | Class II | Active |
| Nitrex | N351454 | FDA UDI | Class II | Active |
| Maxon | 88866704-23 | FDA UDI | Class II | Unknown |
Related Companies
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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. |