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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 22 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| SILS Port | SILSPT15 | FDA UDI | Class II | Unknown |
| iDrive | INTB100 | FDA UDI | Class II | Unknown |
| Shiley | 86045 | FDA UDI | Class II | Active |
| Nellcor | SC-NEO-I | FDA UDI | Class II | Active |
| Puritan Bennett | S-133293-00B | FDA UDI | Class I | Unknown |
| Shiley | 18780 | FDA UDI | Class II | Active |
| Emprint SX | CABK8666L | FDA UDI | Class II | Active |
| Maxon | 8886 6295-61 | FDA UDI | Class II | Unknown |
| Herculon | H0005 | FDA UDI | Class II | Unknown |
| EverCross | AB35W05120135 | FDA UDI | Class II | Active |
| Maxon | 8886612111-2 | FDA UDI | Class II | Active |
| Syneture | US1425 | FDA UDI | Class II | Unknown |
| Caprosyn | GC-323 | FDA UDI | Class II | Active |
| Multifire Endo Hernia | 174027 | FDA UDI | Class II | Active |
| Endo Shears | 174601 | FDA UDI | Class II | Active |
| Edge | E1465NSB | FDA UDI | Class II | Active |
| Tritis | 2621SS | FDA UDI | Class II | Active |
| Nellcor | N600X-1A | FDA UDI | Class II | Unknown |
| Chromic Gut | CG-824L | FDA UDI | Class II | Unknown |
| Polysorb | L-1787K | FDA UDI | Class II | Active |
| Sofsilk | SS-784 | FDA UDI | Class II | Active |
| Puritan Bennett | 980U1PTDIUNA | FDA UDI | Class II | Active |
| Shiley | M4.5NEO | FDA UDI | Class II | Active |
| Sofsilk | SS5676GMDL | FDA UDI | Class II | Unknown |
| Visi-Pro | PXB35-05-57-080 | FDA UDI | Class II | Active |
| Mallinckrodt | 86079 | FDA UDI | Class II | Unknown |
| Ti-Cron | 88863002-62 | FDA UDI | Class II | Active |
| Sonicision | SCDA39 | FDA UDI | U | Active |
| Sofsilk | SS-654 | FDA UDI | Class II | Active |
| Valleylab | E3310 | FDA UDI | Class II | Active |
| Caprosyn | SC-693 | FDA UDI | Class II | Active |
| VersaOne | ONB5STF2C | FDA UDI | Class II | Active |
| Puritan Bennett | 980U1ESDIUU | FDA UDI | Class II | Unknown |
| Ti-Cron | 88863139-21 | FDA UDI | Class II | Active |
| Dar | 444SPA2016 | FDA UDI | Class I | Active |
| V-Loc 180 | VLOCL0224 | FDA UDI | Class II | Active |
| Syneture | US1349A | FDA UDI | Class II | Unknown |
| Maxon | 8886 6235-51 | FDA UDI | Class II | Unknown |
| RapidCross™ | A14BX020100170 | FDA UDI | Class II | Active |
| Puritan Bennett | 980X1PTDIPC | FDA UDI | Class II | Active |
| Chromic Gut | GG-123 | FDA UDI | Class II | Active |
| Ti-Cron | 88863393-51 | FDA UDI | Class II | Active |
| Situate | G0404-32P01CN-1 | FDA UDI | Class I | Active |
| VersaOne | ONB12STS | FDA UDI | Class II | Active |
| Velosorb Fast | CV-1673 | FDA UDI | Class II | Active |
| Plain Gut | SG-5654G | FDA UDI | Class II | Unknown |
| Roticulator | 017617 | FDA UDI | Class II | Unknown |
| Mon-a-Therm | 90052 | FDA UDI | Class II | Active |
| Velosorb Fast | SV-2238 | FDA UDI | Class II | Active |
| Maxon | X-1369 | FDA UDI | Class II | Active |
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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. |