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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 5 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Novafil | 88864490-41 | FDA UDI | Class II | Active |
| Maxon CV | 8886 6121-11 | FDA UDI | Class II | Unknown |
| Monosof | SN-5669 | FDA UDI | Class II | Active |
| Valleylab | E2781R-28ASP | FDA UDI | Class II | Active |
| Ti-Cron | 88863065-61 | FDA UDI | Class II | Active |
| Dar | 444SP02414 | FDA UDI | Class I | Active |
| Visi-Pro™ | PXB35-06-37-080 | FDA UDI | Class II | Active |
| TrailBlazer™ Angled | ASC-035-090 | FDA UDI | Class II | Unknown |
| McGRATH | X3-003-000 | FDA UDI | Class I | Active |
| Auto Suture | 098002 | FDA UDI | Class I | Active |
| Dar | 352/5864 | FDA UDI | Class II | Active |
| EsoFLIP | ES-330 | FDA UDI | Class II | Active |
| Surgipro ll | VPF-612-X | FDA UDI | Class II | Unknown |
| Dar | 331S5686 | FDA UDI | Class I | Active |
| Edge | E1552NSB | FDA UDI | Class II | Active |
| Ti-Cron | 88863084-56 | FDA UDI | Class II | Active |
| Sofsilk | CS-793 | FDA UDI | Class II | Active |
| EverFlex™ | EVD35-07-040-080 | FDA UDI | Class III | Active |
| SpiderFX | SPD2-US-060-190 | FDA UDI | Class II | Active |
| Shiley | 18885 | FDA UDI | Class II | Active |
| Evident | VT1237 | FDA UDI | Class II | Unknown |
| Polysorb | CL-841 | FDA UDI | Class II | Active |
| Ti-Cron | 88863092-71 | FDA UDI | Class II | Active |
| Protege GPS | SERB65-12-20-120 | FDA UDI | Class II | Active |
| Nellcor | MAXFASTI | FDA UDI | Class II | Active |
| Shiley | 6CFN | FDA UDI | Class II | Active |
| Puritan Bennett | 980HFO2T | FDA UDI | Class II | Active |
| VersaOne | RUNVCA8STF | FDA UDI | Class II | Active |
| Barrx | 3441C | FDA UDI | Class II | Unknown |
| Monosof | SN-3686 | FDA UDI | Class II | Active |
| Cool-tip | CTSW Control ZD | FDA UDI | Class II | Active |
| Reliamax | GIA60RS | FDA UDI | Class II | Active |
| EverCross | AB35W04120080 | FDA UDI | Class II | Active |
| Shiley | 86443 | FDA UDI | Class II | Active |
| RapidCross™ | A14BX040100170 | FDA UDI | Class II | Active |
| V-Loc 90 | VLOCM3226 | FDA UDI | Class II | Unknown |
| Velosorb Fast | CV-56 | FDA UDI | Class II | Active |
| Bis | 186-0224-SF | FDA UDI | Class II | Active |
| Puritan Bennett | G-760220NISB-EN | FDA UDI | Class II | Unknown |
| Ti-Cron | XX-5227 | FDA UDI | Class II | Unknown |
| Ti-Cron | 88863379-52 | FDA UDI | Class II | Active |
| Situate | TOR-0101CN-1 | FDA UDI | Class I | Active |
| PowerCross | AB18W060100150 | FDA UDI | Class II | Active |
| Premium Multifire TA | 010316L | FDA UDI | Class II | Unknown |
| Caprosyn | SC-5679 | FDA UDI | Class II | Active |
| Chromic Gut | CG-803 | FDA UDI | Class II | Active |
| Monosof | SN-763 | FDA UDI | Class II | Active |
| Ti-Cron | 88863288-01 | FDA UDI | Class II | Unknown |
| Chromic Gut | G-1766K | FDA UDI | Class II | Active |
| EverCross | AB35W07200080 | 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. |