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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 27 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| EverCross | AB35W07100135 | FDA UDI | Class II | Active |
| GI Genius | CB1708-EU | FDA UDI | Class II | Active |
| Protege RX | SECX-8-30-135 | FDA UDI | Class III | Active |
| Velosorb Fast | SV-9927 | FDA UDI | Class II | Active |
| Ti-Cron | XX-5115 | FDA UDI | Class II | Active |
| Sofsilk | XX-5076 | FDA UDI | Class II | Unknown |
| Biosyn | CM-966 | FDA UDI | Class II | Active |
| Versaport Plus | 179078PF | FDA UDI | Class II | Active |
| Shiley | 96580 | FDA UDI | Class II | Unknown |
| Ti-cron | X-1371 | FDA UDI | Class II | Unknown |
| Monosof | SN-5668 | FDA UDI | Class II | Active |
| Ti-Cron | 88863008-31 | FDA UDI | Class II | Active |
| Valleylab | E3774-36 | FDA UDI | Class II | Active |
| Protege EverFlex | PRB35-05-100-080 | FDA UDI | Class II | Active |
| Versaport Plus | NB12STF | FDA UDI | Class II | Active |
| EverFlex | PRB35-07-030-120 | FDA UDI | Class III | Active |
| Shiley | 110875 | FDA UDI | Class II | Active |
| Endoflip | EF-304 | FDA UDI | Class II | Active |
| Shiley | 6.5PELF | FDA UDI | Class II | Active |
| Maxon | 8886 6217-21 | FDA UDI | Class II | Unknown |
| V-Loc 90 | VLOCM2115 | FDA UDI | Class II | Active |
| Polysorb | XX-5192 | FDA UDI | Class II | Active |
| Polysorb | CL-835-L | FDA UDI | Class II | Active |
| Biosyn | CMT-741-M | FDA UDI | Class II | Active |
| IntraStent LD Max | S18-26 | FDA UDI | Class II | Active |
| AqWire | A181501 | FDA UDI | Class II | Active |
| Shiley | 86652 | FDA UDI | Class II | Unknown |
| Sofsilk | S-1766K | FDA UDI | Class II | Unknown |
| Puritan Bennett | G-061792-00 | FDA UDI | Class II | Unknown |
| Polysorb | SL-632 | FDA UDI | Class II | Active |
| Polysorb | CL-982 | FDA UDI | Class II | Active |
| Extrahand | OMS-EH1 | FDA UDI | Class II | Unknown |
| EndoFLIP | EF-322N | FDA UDI | Class II | Active |
| CleanCoat | E3770-36C | FDA UDI | Class II | Active |
| Tri-Staple 2.0 | SIGTRS60AMT | FDA UDI | Class II | Active |
| Illumisite | ILS-1000-CS | FDA UDI | Class II | Active |
| Kendall | 33136RKT | FDA UDI | Class II | Active |
| Sofsilk | SS-632 | FDA UDI | Class II | Active |
| Dar | 354/5876 | FDA UDI | Class I | Active |
| Shiley | 125139 | FDA UDI | Class II | Active |
| Chemosite | 120020 | FDA UDI | Class II | Unknown |
| Dar | 331/5306 | FDA UDI | Class I | Active |
| Puritan Bennett | 180-05 | FDA UDI | Class II | Active |
| Multifire Endo TA | 010913L | FDA UDI | Class II | Unknown |
| EverCross | AB35W04060135 | FDA UDI | Class II | Active |
| Versaport | NB5STFLP | FDA UDI | Class II | Unknown |
| Ti-Cron | VCD-346 | FDA UDI | Class II | Active |
| Ti-Cron | 88863159-51 | FDA UDI | Class II | Active |
| Edge | E2350HS | FDA UDI | Class II | Active |
| Polysorb | CL-977 | 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. |