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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 39 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Polysorb | CLT-952 | FDA UDI | Class II | Active |
| Valleylab | E7509 | FDA UDI | Class II | Active |
| Puritan Bennett | 980X1ENDIAC | FDA UDI | Class II | Active |
| Surgilon | 88861969-52 | FDA UDI | Class II | Active |
| Ti-Cron | XX-5176 | FDA UDI | Class II | Unknown |
| Polysorb | L-102 | FDA UDI | Class II | Active |
| Shiley | 18775 | FDA UDI | Class II | Active |
| Polysorb | CL-938 | FDA UDI | Class II | Unknown |
| Dar | 354/5414 | FDA UDI | Class I | Active |
| Syneture | US1477 | FDA UDI | Class II | Unknown |
| Maxon | 8886 6245-41 | FDA UDI | Class II | Active |
| Surgiwand II | 178094 | FDA UDI | Class II | Active |
| Polysorb | CL-376-MG | FDA UDI | Class II | Active |
| VersaOne | BPT12STS | FDA UDI | Class II | Active |
| Maxon | 8886 6007-51 | FDA UDI | Class II | Active |
| Syneture | US1413 | FDA UDI | Class II | Unknown |
| Ti-Cron | 88863147-89 | FDA UDI | Class II | Active |
| Surgipro ll | VP-583-X | FDA UDI | Class II | Active |
| Novafil | 8886 4420-23 | FDA UDI | Class II | Active |
| Monosof | SN-5699 | FDA UDI | Class II | Active |
| Shiley | M0NT | FDA UDI | Class II | Active |
| Illumisite | ILS-1000-CS | FDA UDI | Class II | Active |
| LigaSure | LS1500 | FDA UDI | Class II | Active |
| Puritan Bennett | 10114989 | FDA UDI | Class II | Active |
| Dar | R015 | FDA UDI | Class II | Active |
| Shiley | 86199 | FDA UDI | Class II | Active |
| Velosorb Fast | CV-9936G | FDA UDI | Class II | Active |
| Fortrex™ | A35HPV04020135 | FDA UDI | Class II | Active |
| Surgipro ll | CP-413 | FDA UDI | Class II | Unknown |
| Polysorb | CL-885-M | FDA UDI | Class II | Active |
| Dar | 444SP02412 | FDA UDI | Class I | Active |
| Shiley | 96375 | FDA UDI | Class II | Active |
| Polysorb | CL-595 | FDA UDI | Class II | Active |
| Shiley | 7CN80R | FDA UDI | Class II | Active |
| AbsorbaTack | ABSTACK10 | FDA UDI | Class II | Unknown |
| Sofsilk | CS-93-M | FDA UDI | Class II | Unknown |
| Syneture | US1557 | FDA UDI | Class II | Unknown |
| Pi | 4901T | FDA UDI | Class II | Unknown |
| Mallinckrodt | 86122 | FDA UDI | Class II | Unknown |
| Fortrex™ | A35HPV08100080 | FDA UDI | Class II | Active |
| Chromic Gut | SG-1929 | FDA UDI | Class II | Unknown |
| Surgipro ll | VP-975-X | FDA UDI | Class II | Active |
| Edge | E1455-4 | FDA UDI | Class II | Active |
| Maxon | 88866297-11 | FDA UDI | Class II | Unknown |
| Polysorb | UL-046 | FDA UDI | Class II | Active |
| PowerCross | AB18W030120150 | FDA UDI | Class II | Active |
| Sofsilk | VS880-2 | FDA UDI | Class II | Active |
| Polysorb | CL-870 | FDA UDI | Class II | Active |
| Polysorb | CL-527 | FDA UDI | Class II | Unknown |
| SpiderFX | SPD2-US-030-320 | FDA UDI | Class II | Active |
Related Companies
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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. |