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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 10 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nitrex | N181805 | FDA UDI | Class II | Active |
| EverCross | AB35W08040135 | FDA UDI | Class II | Active |
| TrailBlazer™ Angled | ASC-014-090 | FDA UDI | Class II | Unknown |
| Surgilon | 88861918-31 | FDA UDI | Class II | Active |
| Plain Gut | CG-842 | FDA UDI | Class II | Active |
| Situate | VPK-0272C-R | FDA UDI | Class I | Active |
| V-Loc 90 | VLOCM0114 | FDA UDI | Class II | Active |
| Ti-Cron | XX-5059 | FDA UDI | Class II | Active |
| Paramount Mini GPS | PMB8-7-18-80 | FDA UDI | Class II | Active |
| Sofsilk | S-1740K | FDA UDI | Class II | Unknown |
| Shiley | 87455 | FDA UDI | Class II | Active |
| Protege GPS | SERB65-09-20-80 | FDA UDI | Class II | Active |
| Endo GIA | 030450 | FDA UDI | Class II | Unknown |
| LigaSure Atlas | LS1020 | FDA UDI | Class II | Active |
| Ti-Cron | VCD-256 | FDA UDI | Class II | Unknown |
| Biosyn | CM-811 | FDA UDI | Class II | Active |
| Shiley | 8DICFEN | FDA UDI | Class II | Active |
| Sofsilk | VS581-2 | FDA UDI | Class II | Active |
| Shiley | 6FEN | FDA UDI | Class II | Active |
| Shiley | 4DIC | FDA UDI | Class II | Active |
| Spacemaker | SMBTTOVLX | FDA UDI | Class II | Active |
| Shiley | 4.5PDC | FDA UDI | Class II | Active |
| RapidCross™ | A14BX035040090 | FDA UDI | Class II | Active |
| NanoCross™ | AB14W035120090 | FDA UDI | Class II | Unknown |
| Kendall™ | WWTD35001 | FDA UDI | Class II | Active |
| Fortrex | A35HPV04100080 | FDA UDI | Class II | Active |
| Chromic Gut | G-213 | FDA UDI | Class II | Unknown |
| Surgipro II | VP-761-MX | FDA UDI | Class II | Active |
| Puritan Bennett | 980X3CSNISC | FDA UDI | Class II | Active |
| Ti-Cron | 88863043-21 | FDA UDI | Class II | Unknown |
| RapidCross | A14BX035120170 | FDA UDI | Class II | Active |
| Nellcor | D20 | FDA UDI | Class II | Unknown |
| Biosyn | XX-5229J | FDA UDI | Class II | Active |
| Ti-Cron | XX-5058 | FDA UDI | Class II | Active |
| Polysorb | GL-223 | FDA UDI | Class II | Active |
| Polysorb | CL-979 | FDA UDI | Class II | Active |
| Novafil | XX-5011 | FDA UDI | Class II | Active |
| PowerCross | AB18W040200150 | FDA UDI | Class II | Active |
| EverCross | AB35W05030040 | FDA UDI | Class II | Active |
| Versaport Plus | NBFCA12ST | FDA UDI | Class II | Active |
| Ti-Cron | 88863348-31 | FDA UDI | Class II | Active |
| Shiley | 5.5PCF | FDA UDI | Class II | Active |
| Bis | 186-0199-DS | FDA UDI | Class II | Unknown |
| Fortrex | A35HPV08040040 | FDA UDI | Class II | Active |
| Situate | G0404-16P01C-1 | FDA UDI | Class I | Active |
| Surgipro II | XX-5094-L | FDA UDI | Class II | Unknown |
| Nellcor | EASYCAP II | FDA UDI | Class II | Active |
| Monosof | CN-791 | FDA UDI | Class II | Active |
| Valleylab | E3530-3 | FDA UDI | Class II | Active |
| Dar | 444S02806 | FDA UDI | Class I | 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. |