Is this your brand? Sign in to claim ownership.
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 36 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Puritan Bennett | 980S3ESDIUU | FDA UDI | Class II | Active |
| Puritan Bennett | 980X1ENAIQC | FDA UDI | Class II | Active |
| VersaOne | RNONB12LGF | FDA UDI | Class II | Unknown |
| Surgiwip | EDW-51 | FDA UDI | Class II | Active |
| Biosyn | CM-954 | FDA UDI | Class II | Active |
| Polysorb | CL-16-MG | FDA UDI | Class II | Active |
| Ti-Cron | 88863113-71 | FDA UDI | Class II | Active |
| EndoFLIP | EF-100 | FDA UDI | Class II | Active |
| Sofsilk | S-1769K | FDA UDI | Class II | Active |
| Vital Sync | VITALSYNCSW03 | FDA UDI | Class II | Active |
| VersaOne | ONB11LGF | FDA UDI | Class II | Active |
| Shiley | M4DFEN | FDA UDI | Class II | Active |
| Shiley | 86349 | FDA UDI | Class II | Active |
| V-Loc 180 | VLOCL0346 | FDA UDI | Class II | Active |
| Sofsilk | XX-5284 | FDA UDI | Class II | Active |
| Biosyn | CM-843 | FDA UDI | Class II | Active |
| Monosof | SN-728 | FDA UDI | Class II | Active |
| Protege EverFlex | PRB35-05-030-120 | FDA UDI | Class II | Active |
| Shiley | 86398 | FDA UDI | Class II | Active |
| Mallinckrodt | 96380 | FDA UDI | Class II | Active |
| Surgipro II | VP-556MX | FDA UDI | Class II | Active |
| Dar | 444SP02016 | FDA UDI | Class I | Active |
| Step | S110000 | FDA UDI | Class II | Active |
| RapidCross™ | A14BX025080170 | FDA UDI | Class II | Active |
| Shiley | 9CN90ES | FDA UDI | Class II | Unknown |
| Mallinckrodt | 96580 | FDA UDI | Class II | Unknown |
| Valleylab | SEP5000 | FDA UDI | Class II | Unknown |
| Tri-Staple 2.0 | SIGTRSB60AMT | FDA UDI | Class II | Active |
| Shiley | 4FENJ-S | FDA UDI | Class II | Active |
| Veriset | HP0510E | FDA UDI | Class III | Active |
| Tri-Staple 2.0 | SIGCIR21MT | FDA UDI | Class II | Active |
| RapidCross™ | A14BX040100090 | FDA UDI | Class II | Active |
| Surgipro ll | VP-719-MX | FDA UDI | Class II | Active |
| Endo Clip | 176500 | FDA UDI | Class II | Unknown |
| Puritan Bennett | 10051468 | FDA UDI | Class II | Unknown |
| PowerCross | AB18W050200150 | FDA UDI | Class II | Active |
| Sofsilk | XX-5081 | FDA UDI | Class II | Unknown |
| Chromic Gut | CG-49 | FDA UDI | Class II | Active |
| Steel | XX-2125 | FDA UDI | Class II | Unknown |
| Ti-Cron | XX-5126 | FDA UDI | Class II | Active |
| Polysorb | SL-642 | FDA UDI | Class II | Active |
| Polysorb | SL-1645G | FDA UDI | Class II | Active |
| Monosof | CN-819 | FDA UDI | Class II | Active |
| Extra View | OMS-XB1 | FDA UDI | Class II | Active |
| Chromic Gut | G-254 | FDA UDI | Class II | Active |
| Polysorb | SL-1659 | FDA UDI | Class II | Active |
| Polysorb | L-38 | FDA UDI | Class II | Active |
| Surgipro ll | SP-5680G | FDA UDI | Class II | Active |
| Mallinckrodt | 109880 | FDA UDI | Class II | Active |
| Shiley | M8DCFS | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
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. |