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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 6 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| VersaOne | B12STS | FDA UDI | Class II | Active |
| Ti-Cron | 88863353-56 | FDA UDI | Class II | Active |
| EverCross | AB35W06200080 | FDA UDI | Class II | Active |
| Shiley | 5.5PEF | FDA UDI | Class II | Active |
| Dar | R002 | FDA UDI | Class II | Active |
| Nitrex | N351805 | FDA UDI | Class II | Active |
| Syneture | US1714 | FDA UDI | Class II | Unknown |
| superDimension | ILS-0001-FN | FDA UDI | Class II | Active |
| Surgipro II | X1379 | FDA UDI | Class II | Unknown |
| Puritan Bennett | 980X1ITDISS | FDA UDI | Class II | Active |
| Nitrex | N251802 | FDA UDI | Class II | Active |
| Nellcor | MAXIR | FDA UDI | Class II | Active |
| Shiley | 8LPC-S | FDA UDI | Class II | Active |
| Sofsilk | CS-425 | FDA UDI | Class II | Active |
| Visi-Pro | PXB35-07-27-080 | FDA UDI | Class II | Active |
| TrailBlazer™ Angled | ASC-035-135 | FDA UDI | Class II | Active |
| Shiley | 86005 | FDA UDI | Class II | Unknown |
| Situate | L1818-04P02C-1 | FDA UDI | Class I | Active |
| Monosof | N-2500 | FDA UDI | Class II | Active |
| Lapro-Clip | 8886848508 | FDA UDI | Class II | Unknown |
| Surgipro II | VP-756-X | FDA UDI | Class II | Unknown |
| Situate | G0303-12P01C-1 | FDA UDI | Class I | Active |
| Polysorb | SL-5633 | FDA UDI | Class II | Active |
| Surgipro ll | SP-5698 | FDA UDI | Class II | Active |
| Sofsilk | VS-671 | FDA UDI | Class II | Unknown |
| Sofsilk | SS-5676 | FDA UDI | Class II | Active |
| Versaport | 177772 | FDA UDI | Class II | Active |
| Surgipro | VP-897-M | FDA UDI | Class II | Unknown |
| Puritan Bennett | 980X1ENDIPB | FDA UDI | Class II | Active |
| Polysorb | L-42 | FDA UDI | Class II | Active |
| LigaSure XP | LXMJ23L | FDA UDI | Class II | Active |
| Chromic Gut | SG-634 | FDA UDI | Class II | Active |
| Polysorb | LL-101 | FDA UDI | Class II | Active |
| Ti-Cron | 88863001-62 | FDA UDI | Class II | Active |
| Shiley | 9CN90ER | FDA UDI | Class II | Active |
| Mallinckrodt | 86451 | FDA UDI | Class II | Active |
| Monosof | SN-3965 | FDA UDI | Class II | Active |
| Paramount Mini GPS | PMB4-7-14-80 | FDA UDI | Class II | Active |
| Dar | 444S02606 | FDA UDI | Class I | Active |
| Syneture | US1577 | FDA UDI | Class II | Unknown |
| SILS Stitch | SILSSTITCH | FDA UDI | Class II | Unknown |
| Invos | IS | FDA UDI | Class II | Active |
| LigaSure | LF1212A | FDA UDI | Class II | Active |
| Ti-Cron | VCD2346 | FDA UDI | Class II | Unknown |
| Nellcor | DEC4 | FDA UDI | Class II | Active |
| LigaSure | LF5637 | FDA UDI | Class II | Active |
| Sofsilk | SS-522 | FDA UDI | Class II | Unknown |
| Shiley | 5CN70A | FDA UDI | Class II | Active |
| Sofsilk | SS-591 | FDA UDI | Class II | Unknown |
| Sofsilk | S-195 | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
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Importers
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Notified Bodies
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Authorities
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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. |