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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 13 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| ManoScan | 9012P1422 | FDA UDI | Class II | Unknown |
| Polysorb | SL-638 | FDA UDI | Class II | Active |
| Dar | 444SPY2314 | FDA UDI | Class I | Active |
| BioTritis | 2140SS | FDA UDI | Class I | Active |
| Polysorb | SL-712 | FDA UDI | Class II | Active |
| Puritan Bennett | 10049999 | FDA UDI | Class II | Unknown |
| PowerCross | AB18W030020090 | FDA UDI | Class II | Active |
| ProTack | 174006 | FDA UDI | Class II | Active |
| PowerCross | AB18W050020090 | FDA UDI | Class II | Active |
| Visi-Pro | PXB35-07-12-080 | FDA UDI | Class II | Active |
| PowerCross | AB18W060100090 | FDA UDI | Class II | Active |
| Valleylab | E2516 | FDA UDI | Class II | Active |
| Polysorb | GL-130 | FDA UDI | Class II | Unknown |
| Biosyn | XX-5243 | FDA UDI | Class II | Unknown |
| Puritan Bennett | 4-840120DIUU-SP | FDA UDI | Class II | Unknown |
| Sofsilk | SS-5640 | FDA UDI | Class II | Active |
| Microstream | PMC40M | FDA UDI | Class II | Active |
| RapidCross™ | A14BX030060170 | FDA UDI | Class II | Active |
| Velosorb Fast | CV-3110 | FDA UDI | Class II | Active |
| Ti-Cron | 88863249-31 | FDA UDI | Class II | Active |
| EverFlex | PRB35-07-040-080 | FDA UDI | Class III | Active |
| McGRATH MAC | 350-088-000 | FDA UDI | Class I | Active |
| Monosof | SN-615 | FDA UDI | Class II | Active |
| Mallinckrodt | 86469 | FDA UDI | Class II | Unknown |
| Surgipro | X-1002 | FDA UDI | Class II | Unknown |
| Surgipro II | XX-5205J | FDA UDI | Class II | Unknown |
| Polysorb | 3-CL-812 | FDA UDI | Class II | Unknown |
| Visi-Pro™ | PXB35-05-17-135 | FDA UDI | Class III | Active |
| Mallinckrodt | 86460 | FDA UDI | Class II | Unknown |
| Dar | 444SP03014 | FDA UDI | Class I | Active |
| LigaSure | LF1212A | FDA UDI | Class II | Active |
| Endo Stitch | 173016 | FDA UDI | Class II | Active |
| Surgipro II | X1401 | FDA UDI | Class II | Unknown |
| Endo GIA | EGIA45AMT | FDA UDI | Class II | Active |
| Emprint | CAMPA | FDA UDI | Class II | Unknown |
| Puritan Bennett | 980U3PTDIUNA | FDA UDI | Class II | Active |
| Emprint | CART1 | FDA UDI | Class II | Active |
| Nellcor | MAXAR | FDA UDI | Class II | Active |
| RapidCross | A14BX020040090 | FDA UDI | Class II | Active |
| RapidCross | A14BX040040090 | FDA UDI | Class II | Active |
| Polysorb | CL-030 | FDA UDI | Class II | Active |
| Newport | DLHT50-H1-B | FDA UDI | Class II | Active |
| Surgipro ll | VP-941-X | FDA UDI | Class II | Active |
| RapidCross | A14BX040210090 | FDA UDI | Class II | Active |
| Puritan Bennett | 10097559 | FDA UDI | Class II | Active |
| Dar | 444SPY2312 | FDA UDI | Class I | Active |
| Bis | 186-0224-NK-RFB | FDA UDI | Class II | Active |
| Monosof | SN-5660G | FDA UDI | Class II | Active |
| Stratis | 2064SS | FDA UDI | Class I | Unknown |
| Endo Clip MultApplier | 500-11A | FDA UDI | Class II | Unknown |
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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. |