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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 17 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Polysorb | 170094 | FDA UDI | Class II | Active |
| Duraseal | 20-2050 | FDA UDI | Class III | Unknown |
| Syneture | US1731 | FDA UDI | Class II | Unknown |
| Mon-a-Therm | 502-0410A | FDA UDI | Class II | Active |
| Dar | 351P5980 | FDA UDI | Class II | Active |
| VersaStep | VSR107005 | FDA UDI | Class II | Unknown |
| Shiley | 6DICFEN | FDA UDI | Class II | Active |
| Polysorb | 273022 | FDA UDI | Class II | Unknown |
| Mallinckrodt | 86108 | FDA UDI | Class II | Active |
| EverCross | AB35W04030135 | FDA UDI | Class II | Active |
| Mallinckrodt | 5-18437 | FDA UDI | Class II | Active |
| Surgilon | 88861962-72 | FDA UDI | Class II | Active |
| Multifire Endo GIA | 030807L | FDA UDI | Class II | Unknown |
| Eea | EEA21 | FDA UDI | Class II | Active |
| Velosorb Fast | SV-1290 | FDA UDI | Class II | Active |
| Caprosyn | SC-3634 | FDA UDI | Class II | Active |
| Surgilon | 88861951-61 | FDA UDI | Class II | Active |
| Surgipro II | X-1358 | FDA UDI | Class II | Unknown |
| Shiley | M6FEN | FDA UDI | Class II | Active |
| Dar | 353S19046 | FDA UDI | Class I | Active |
| Mallinckrodt | 86455 | FDA UDI | Class II | Active |
| Dar | 444SP02116 | FDA UDI | Class I | Active |
| Shiley | 125028 | FDA UDI | Class II | Active |
| Shiley | M5.0PED | FDA UDI | Class II | Active |
| Tri-Staple 2.0 | SIG30CTAVM | FDA UDI | Class II | Active |
| Maxon | X1392 | FDA UDI | Class II | Active |
| Evident | VTUBE | FDA UDI | Class II | Unknown |
| Dar | 350U5879 | FDA UDI | Class II | Active |
| Vascufil | 88864701-05V | FDA UDI | Class II | Unknown |
| Shiley | 126139 | FDA UDI | Class II | Active |
| Situate | TST-1250C-1 | FDA UDI | Class I | Active |
| Fortrex™ | A35HPV04080040 | FDA UDI | Class II | Active |
| Shiley | SSVO | FDA UDI | Class II | Active |
| Valleylab | E2504H | FDA UDI | Class II | Unknown |
| Bis | 186-0224-SF-RFB | FDA UDI | Class II | Active |
| V-Loc 180 | VLOCL0814 | FDA UDI | Class II | Active |
| Cool-tip | ACT2530 | FDA UDI | Class II | Active |
| Mallinckrodt | 86653 | FDA UDI | Class II | Unknown |
| Puritan Bennett | 980X1JADIJJ | FDA UDI | Class II | Active |
| Multifire Premium | 059035 | FDA UDI | Class I | Active |
| Protege GPS | SERB65-14-20-120 | FDA UDI | Class II | Active |
| Mallinckrodt | 86208 | FDA UDI | Class II | Unknown |
| Illumisite | ILS-2200-BA | FDA UDI | Class II | Active |
| Multifire Endo GIA | 030811 | FDA UDI | Class II | Unknown |
| EverCross | AB35W10030135 | FDA UDI | Class II | Active |
| Emprint | CA30L2 | FDA UDI | Class II | Active |
| Shiley | M6DCFS | FDA UDI | Class II | Active |
| SurgiStat | VLSURGGENZE | FDA UDI | Class II | Active |
| Puritan Bennett | 980X1ENNISP | FDA UDI | Class II | Unknown |
| Ti-Cron | 88863374-62 | 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. |