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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 38 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Fortrex | A35HPV09080040 | FDA UDI | Class II | Active |
| Surgipro II | VP-209MX | FDA UDI | Class II | Active |
| Shiley | M8LPC | FDA UDI | Class II | Active |
| Valleylab | VL2610DB | FDA UDI | Class II | Active |
| V-Loc | VLOCN0604 | FDA UDI | Class II | Active |
| Emprint | CA20L2 | FDA UDI | Class II | Active |
| Syneture | US1658 | FDA UDI | Class II | Unknown |
| RapidCross™ | A14BX035210090 | FDA UDI | Class II | Active |
| Shiley | 18865S | FDA UDI | Class II | Active |
| Velosorb Fast | CV-947 | FDA UDI | Class II | Active |
| Shiley | M10CFN | FDA UDI | Class II | Active |
| Polysorb | CLS-812 | FDA UDI | Class II | Unknown |
| Chromic Gut | CG-964 | FDA UDI | Class II | Active |
| Syneture | US1300 | FDA UDI | Class II | Unknown |
| Vascufil | 88864734-21V | FDA UDI | Class II | Unknown |
| Syneture | US1621 | FDA UDI | Class II | Unknown |
| ReliaTack | RELTACK3X10 | FDA UDI | Class II | Active |
| Nitrex | N140801 | FDA UDI | Class II | Active |
| WarmTouch | 502-2100 | FDA UDI | Class II | Unknown |
| Dar | R019 | FDA UDI | Class II | Unknown |
| Bis | 186-0128 | FDA UDI | Class II | Unknown |
| Versaport | 177771 | FDA UDI | Class II | Unknown |
| TA Premium | 010450 | FDA UDI | Class I | Active |
| Valleylab | E1567 | FDA UDI | Class II | Active |
| Fortrex™ | A35HPV10080040 | FDA UDI | Class II | Active |
| ClosureFast | CF7-3-60 | FDA UDI | Class II | Active |
| Newport | MXL70A-GR-DS | FDA UDI | Class II | Active |
| SpiderFX | SPD2-US-070-190 | FDA UDI | Class II | Active |
| Maxon | 8886 6532-21 | FDA UDI | Class II | Active |
| RapidCross™ | A14BX025210090 | FDA UDI | Class II | Active |
| Fortrex™ | A35HPV08100135 | FDA UDI | Class II | Active |
| Visi-Pro™ | PXB35-10-27-135 | FDA UDI | Class II | Active |
| Shiley | 86291 | FDA UDI | Class II | Unknown |
| Biosyn | CM-436 | FDA UDI | Class II | Active |
| Valleylab | SEP6015NSB | FDA UDI | Class II | Active |
| Shiley | 3.0NCF | FDA UDI | Class II | Active |
| Flexon | 88862591-43 | FDA UDI | Class II | Active |
| Caprosyn | UC-246 | FDA UDI | Class II | Unknown |
| Puritan Bennett | 980N3PTDIUNA | FDA UDI | Class II | Unknown |
| NanoCross™ | AB14W035020090 | FDA UDI | Class II | Unknown |
| Ti-Cron | 88863375-71 | FDA UDI | Class II | Active |
| Ti-Cron | XX-5223 | FDA UDI | Class II | Unknown |
| Ti-Cron | 88863035-51 | FDA UDI | Class II | Active |
| Nellcor | MAXR | FDA UDI | Class II | Active |
| Mallinckrodt | 86267 | FDA UDI | Class II | Active |
| Shiley | 8DFEN | FDA UDI | Class II | Active |
| Syneture | US1687 | FDA UDI | Class II | Active |
| EverFlex | PRB35-06-020-080 | FDA UDI | Class III | Active |
| Monosof | SN-788 | FDA UDI | Class II | Active |
| Chromic Gut | CG-10M | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
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Importers
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Notified Bodies
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Authorities
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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. |