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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 19 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Emprint | CAMPP | FDA UDI | Class II | Unknown |
| Dar | 331/5345 | FDA UDI | Class I | Active |
| Dar | 444S02806 | FDA UDI | Class I | Active |
| SpiderFX | SPD2-US-070-320 | FDA UDI | Class II | Active |
| Premium Plus CEEA | 111983 | FDA UDI | Class II | Active |
| Puritan Bennett | 4-840120DIUU-US | FDA UDI | Class II | Unknown |
| Velosorb Fast | CV-9007G | FDA UDI | Class II | Active |
| Polysorb | SL-635G | FDA UDI | Class II | Active |
| Polysorb | SL-1614G | FDA UDI | Class II | Active |
| Surgipro | CP-845 | FDA UDI | Class II | Active |
| Shiley | 3.0NEF | FDA UDI | Class II | Active |
| Valleylab | E4051-CT | FDA UDI | Class II | Active |
| Microstream Advance | ZMVAO | FDA UDI | Class II | Active |
| Puritan Bennett | 4-840220DIPC-PL | FDA UDI | Class II | Unknown |
| Surgilon | 88861984-52 | FDA UDI | Class II | Unknown |
| Endo Clip MultApplier | 500-10A | FDA UDI | Class II | Active |
| Situate | L1836-04P01C-1 | FDA UDI | Class I | Active |
| Polysorb | LL-112 | FDA UDI | Class II | Active |
| V-Loc 180 | VLOCL0133 | FDA UDI | Class II | Active |
| Shiley | 86468 | FDA UDI | Class II | Unknown |
| Biosyn | UM-808 | FDA UDI | Class II | Unknown |
| Dar | R024 | FDA UDI | Class II | Active |
| Polysorb | CL-53 | FDA UDI | Class II | Active |
| Puritan Bennett | 980S3FRDICU | FDA UDI | Class II | Unknown |
| Fortrex | A35HPV06020135 | FDA UDI | Class II | Active |
| EverCross | AB35W09030080 | FDA UDI | Class II | Active |
| Protege RX | SECX-6-30-135 | FDA UDI | Class III | Active |
| RapidCross™ | A14BX020210090 | FDA UDI | Class II | Active |
| Valleylab | E0600 | FDA UDI | Class II | Unknown |
| Biosyn | SM-5678 | FDA UDI | Class II | Active |
| Biosyn | XM-845 | FDA UDI | Class II | Unknown |
| Puritan Bennett | 10122271 | FDA UDI | Class II | Unknown |
| Situate | 01-0044 | FDA UDI | Class I | Active |
| RapidCross™ | A14BX030210170 | FDA UDI | Class II | Active |
| Shiley | 8DCT | FDA UDI | Class II | Unknown |
| OxiMax | N65P | FDA UDI | Class II | Unknown |
| Chromic Gut | SG-5163G | FDA UDI | Class II | Active |
| EverCross | AB35W05060080 | FDA UDI | Class II | Active |
| RapidCross™ | A14BX025080170 | FDA UDI | Class II | Active |
| Fortrex | A35HPV07080080 | FDA UDI | Class II | Active |
| EverCross | AB35W06060080 | FDA UDI | Class II | Active |
| Maxon | 8886 6143-31 | FDA UDI | Class II | Active |
| Sofsilk | XX-5285 | FDA UDI | Class II | Active |
| Shiley | 3.0PEF | FDA UDI | Class II | Active |
| Situate | VPK-0448C-F | FDA UDI | Class I | Active |
| RapidCross™ | A14BX040020090 | FDA UDI | Class II | Active |
| PowerCross | AB18W020100150 | FDA UDI | Class II | Active |
| Puritan Bennett | 980S3ESDIUC | FDA UDI | Class II | Active |
| Het | 180-1022 | FDA UDI | Class II | Active |
| Shiley | M6DCFN | 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. |