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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 37 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Polysorb | GL-47-MG | FDA UDI | Class II | Active |
| Shiley | 18790S | FDA UDI | Class II | Active |
| Cool-tip | CTRF 117ZE | FDA UDI | Class II | Unknown |
| AbsorbaTack | ABSTACK30X | FDA UDI | Class II | Active |
| Dar | 444SP01010 | FDA UDI | Class I | Active |
| Puritan Bennett | 10047078 | FDA UDI | Class I | Active |
| Shiley | 76265 | FDA UDI | Class II | Active |
| Endo GIA | 030459 | FDA UDI | Class II | Active |
| Syneture | US1446 | FDA UDI | Class II | Unknown |
| Caprosyn | UC-879 | FDA UDI | Class II | Active |
| Monosof | CN-825 | FDA UDI | Class II | Active |
| Syneture | US1601 | FDA UDI | Class II | Unknown |
| Surgipro ll | SP-5686 | FDA UDI | Class II | Active |
| Fortrex | A35HPV07040080 | FDA UDI | Class II | Active |
| RapidCross™ | A14BX035080170 | FDA UDI | Class II | Active |
| Versaport | 179093F | FDA UDI | Class II | Active |
| RapidCross™ | A14BX035120090 | FDA UDI | Class II | Active |
| Mon-a-Therm | 90058 | FDA UDI | Class II | Active |
| Novafil | PB-6713K | FDA UDI | Class II | Active |
| Puritan Bennett | 4-074605-00 | FDA UDI | Class II | Unknown |
| Surgilon | 88861964-51 | FDA UDI | Class II | Active |
| Novafil | X-1321 | FDA UDI | Class II | Unknown |
| Plain Gut | GG-321 | FDA UDI | Class II | Active |
| Biosyn | CM-801 | FDA UDI | Class II | Active |
| Endo Close | 173022 | FDA UDI | Class II | Active |
| EverCross | AB35W03020080 | FDA UDI | Class II | Active |
| Syneture | US1590 | FDA UDI | Class II | Unknown |
| Monosof | CN-771 | FDA UDI | Class II | Active |
| Chromic Gut | G-214 | FDA UDI | Class II | Unknown |
| Dar | 444SP02016 | FDA UDI | Class I | Active |
| Surgipro | SMHP-01 | FDA UDI | Class II | Active |
| Puritan Bennett | 4-840220DIPC-PR | FDA UDI | Class II | Unknown |
| PowerCross | AB18W050060150 | FDA UDI | Class II | Active |
| Valleylab | E2515HS | FDA UDI | Class II | Active |
| Shiley | 10DCFS | FDA UDI | Class II | Unknown |
| Edge | E1455NSB | FDA UDI | Class II | Active |
| Novafil | XNF-1964 | FDA UDI | Class II | Unknown |
| RapidCross™ | A14BX030020090 | FDA UDI | Class II | Active |
| Ti-Cron | 88863261-72 | FDA UDI | Class II | Active |
| Visi-Pro | PXB35-09-27-080 | FDA UDI | Class II | Active |
| Monosof | SN-673 | FDA UDI | Class II | Active |
| Surgitie | EL-23-LN | FDA UDI | Class II | Active |
| V-Loc 180 | VLOCL0624 | FDA UDI | Class II | Active |
| Endo GIA | EGIA45CTAVM | FDA UDI | Class II | Active |
| Surgipro | XX2219 | FDA UDI | Class II | Active |
| Monosof | SN-1854 | FDA UDI | Class II | Unknown |
| Sofsilk | CS-1193-M | FDA UDI | Class II | Unknown |
| Monosof | N-2547 | FDA UDI | Class II | Active |
| Monosof | CN-824 | FDA UDI | Class II | Active |
| Surgipro II | VP713MX-2 | 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. |