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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 18 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Microstream Advance | ZMVAOL | FDA UDI | Class II | Active |
| Polysorb | LL-103 | FDA UDI | Class II | Active |
| HawkOne™ | H1-M | FDA UDI | Class II | Active |
| Surgipro II | XX-5177 | FDA UDI | Class II | Unknown |
| V-Loc | VLOCN304L | FDA UDI | Class II | Active |
| Endo Clip III | 176630B | FDA UDI | Class I | Active |
| Polysorb | L-2 | FDA UDI | Class II | Active |
| Versaport Plus | 179097PF | FDA UDI | Class II | Active |
| Nellcor | DL10076644 | FDA UDI | Class II | Unknown |
| Ti-Cron | 88863220-56 | FDA UDI | Class II | Active |
| Surgipro | XX-5246 | FDA UDI | Class II | Active |
| Maxon | 8886 6245-61 | FDA UDI | Class II | Active |
| Versaport Plus | 177091PF | FDA UDI | Class II | Active |
| Nellcor | PMC10NCH-GE | FDA UDI | Class II | Active |
| Surgipro | VP-151 | FDA UDI | Class II | Active |
| Dar | R013 | FDA UDI | Class II | Active |
| Shiley | M6CFS | FDA UDI | Class II | Active |
| Shiley | 8SIC | FDA UDI | Class II | Active |
| Shiley | M6LGT | FDA UDI | Class II | Active |
| Surgilon | X-1119 | FDA UDI | Class II | Active |
| SurgiSleeve | WPMD509 | FDA UDI | Class II | Active |
| Nellcor | DS100A-1 | FDA UDI | Class II | Active |
| TruClear | 72203606 | FDA UDI | Class II | Active |
| V-Loc 180 | VLOCL0325 | FDA UDI | Class II | Active |
| Novafil | 8886 4424-31 | FDA UDI | Class II | Active |
| Mallinckrodt | 86098 | FDA UDI | Class II | Unknown |
| Mallinckrodt | 18795 | FDA UDI | Class II | Active |
| Dar | 444SP02112 | FDA UDI | Class I | Active |
| Ti-Cron | VCD20305FE | FDA UDI | Class II | Active |
| Puritan Bennett | 980U1ENDIUU | FDA UDI | Class II | Active |
| Premium Surgiclip | 134044 | FDA UDI | Class II | Active |
| Syneture | US1592 | FDA UDI | Class II | Unknown |
| Polysorb | EL-415 | FDA UDI | Class II | Active |
| superDimension | AKI00133-01 | FDA UDI | Class II | Active |
| Syneture | US1672 | FDA UDI | Class II | Unknown |
| McGRATH MAC | 350-013-000 | FDA UDI | Class I | Active |
| Puritan Bennett | 980NIVPLUS | FDA UDI | Class II | Active |
| Biosyn | GM-322 | FDA UDI | Class II | Active |
| Invos | PMPAMP71 | FDA UDI | Class II | Active |
| Polysorb | SL-1510G | FDA UDI | Class II | Active |
| Caprosyn | SC-5618G | FDA UDI | Class II | Active |
| RapidCross™ | A14BX020210090 | FDA UDI | Class II | Active |
| Ti-Cron | 88862775-21 | FDA UDI | Class II | Active |
| Vital Sync | VSMASW04 | FDA UDI | Class II | Active |
| SilverHawkTM | P4055 | FDA UDI | Class II | Active |
| V-Loc 90 | VLOCM1744 | FDA UDI | Class II | Active |
| GIA Premium | 030470 | FDA UDI | Class I | Active |
| ForceTriad | FT6009 | FDA UDI | Class II | Active |
| Novafil | 8886 4401-13 | FDA UDI | Class II | Active |
| Surgipro ll | VP-702-X | 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. |