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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 35 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Polysorb | CL-917 | FDA UDI | Class II | Active |
| Surgipro ll | VP-585-X | FDA UDI | Class II | Active |
| Polysorb | CL-538 | FDA UDI | Class II | Active |
| Ti-Cron | 88863090-51 | FDA UDI | Class II | Active |
| Biosyn | CM-904 | FDA UDI | Class II | Active |
| EverFlex | PRB35-08-150-120 | FDA UDI | Class III | Active |
| Nitrex | N252601 | FDA UDI | Class II | Active |
| Invos | PMAC71DOC | FDA UDI | Class II | Active |
| Situate | PPK-025YC-R | FDA UDI | Class I | Active |
| Maxon | 8886 6245-71 | FDA UDI | Class II | Active |
| Puritan Bennett | 4-076442-00 | FDA UDI | Class II | Unknown |
| Shiley | M4DCT | FDA UDI | Class II | Active |
| TrailBlazer™Angled | ASC-018-150 | FDA UDI | Class II | Active |
| EverCross | AB35W06030080 | FDA UDI | Class II | Active |
| Surgipro | SPMM-66 | FDA UDI | Class II | Active |
| Tritis | 2153SS | FDA UDI | Class II | Unknown |
| Ti-Cron | 88863062-41 | FDA UDI | Class II | Active |
| Syneture | US1588 | FDA UDI | Class II | Unknown |
| Nitrex | N351455 | FDA UDI | Class II | Active |
| Mallinckrodt | 86111 | FDA UDI | Class II | Active |
| Surgiwand II | 178082 | FDA UDI | Class II | Unknown |
| Polysorb | CL-976 | FDA UDI | Class II | Active |
| Chromic Gut | CG-913 | FDA UDI | Class II | Active |
| Biosyn | GM-291 | FDA UDI | Class II | Active |
| VersaStep | VSR100712 | FDA UDI | Class II | Unknown |
| Velosorb Fast | SV-2252 | FDA UDI | Class II | Active |
| Polysorb | CLT-11-MG | FDA UDI | Class II | Active |
| Ti-Cron | 88863261-82 | FDA UDI | Class II | Active |
| Dar | 352/5855 | FDA UDI | Class II | Active |
| Ti-Cron | XX-5063 | FDA UDI | Class II | Unknown |
| Vloc 90 | VLOCM2136 | FDA UDI | Class II | Active |
| Mallinckrodt | 86290 | FDA UDI | Class II | Unknown |
| Fortrex | A35HPV04040040 | FDA UDI | Class II | Active |
| Mallinckrodt | 86287 | FDA UDI | Class II | Active |
| Cool-tip | ACT2030 | FDA UDI | Class II | Active |
| Maxon | 8886 6233-31 | FDA UDI | Class II | Active |
| Surgipro ll | VP-708-X | FDA UDI | Class II | Active |
| Gia | GIA60TMS | FDA UDI | Class II | Active |
| Ti-Cron | 88863111-79 | FDA UDI | Class II | Active |
| Mallinckrodt | 96110 | FDA UDI | Class II | Unknown |
| Monosof | SN-1689G | FDA UDI | Class II | Active |
| Maxon | 8886 6908-31 | FDA UDI | Class II | Active |
| Caprosyn | CC-983 | FDA UDI | Class II | Active |
| Ti-Cron | VCD-2114 | FDA UDI | Class II | Unknown |
| Polysorb | SL-692 | FDA UDI | Class II | Active |
| RapidCross | A14BX040080090 | FDA UDI | Class II | Active |
| Sofsilk | GSJ47M-2 | FDA UDI | Class II | Active |
| ClosureFast | CB-CO-4 x 5 | FDA UDI | Class I | Unknown |
| Polysorb | CL-596 | FDA UDI | Class II | Active |
| Endo GIA | EGIA45AV | FDA UDI | Class II | 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. |