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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 32 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Valleylab | E7509B | FDA UDI | Class II | Active |
| Biosyn | CM-951 | FDA UDI | Class II | Active |
| Vascufil | 8886473931V-2 | FDA UDI | Class II | Unknown |
| AbsorbaTack | ABSTACK20S | FDA UDI | Class II | Active |
| Puritan Bennett | 4-006308-00 | FDA UDI | Class II | Active |
| Polysorb | CL-906 | FDA UDI | Class II | Active |
| Biosyn | UM-886 | FDA UDI | Class II | Active |
| RapidCross™ | A14BX025020170 | FDA UDI | Class II | Active |
| Dar | 444SP01112 | FDA UDI | Class I | Active |
| Bis | 186-0195-uPH | FDA UDI | Class II | Active |
| Velosorb Fast | SV-4431 | FDA UDI | Class II | Active |
| Valleylab | E4059-CT | FDA UDI | Class II | Active |
| Shiley | 86462 | FDA UDI | Class II | Unknown |
| AqWire | A181501 | FDA UDI | Class II | Active |
| Syneture | US1667 | FDA UDI | Class II | Unknown |
| IntraStent LD Mega | S17-16 | FDA UDI | Class II | Active |
| Shiley | 109850 | FDA UDI | Class II | Unknown |
| Ti-Cron | 88863129-51 | FDA UDI | Class II | Active |
| Polysorb | CL-644-M | FDA UDI | Class II | Active |
| Puritan Bennett | 4-076322-00 | FDA UDI | Class II | Unknown |
| Syneture | US1506A | FDA UDI | Class II | Unknown |
| Velosorb Fast | SV-426 | FDA UDI | Class II | Active |
| Monosof | CN-724 | FDA UDI | Class II | Active |
| Shiley | 3.5PEF | FDA UDI | Class II | Active |
| RapidCross | A14BX030120170 | FDA UDI | Class II | Active |
| Shiley | 18755 | FDA UDI | Class II | Active |
| Shiley | 8UN85R | FDA UDI | Class II | Active |
| Surgipro ll | VPF-735-X | FDA UDI | Class II | Active |
| Vascufil | 88864703-11V | FDA UDI | Class II | Unknown |
| ManoScan | 9012P1212 | FDA UDI | Class II | Unknown |
| Shiley | 5CN70ER | FDA UDI | Class II | Active |
| Sofsilk | SS-678 | FDA UDI | Class II | Active |
| RapidCross | A14BX020120090 | FDA UDI | Class II | Active |
| Protege GPS | SERB65-14-20-80 | FDA UDI | Class II | Active |
| Puritan Bennett | 980X3ENNISB | FDA UDI | Class II | Active |
| Novafil | 8886 4450-41 | FDA UDI | Class II | Active |
| Dar | 444S02710 | FDA UDI | Class I | Active |
| Maxon | SMM-5431 | FDA UDI | Class II | Active |
| Endo Clip | 176620 | FDA UDI | Class II | Unknown |
| McGRATH MAC | 350-005-000 | FDA UDI | Class I | Active |
| V-Loc | VLOCN0814 | FDA UDI | Class II | Active |
| Chemosite | 120068 | FDA UDI | Class II | Unknown |
| Sofsilk | SS-623 | FDA UDI | Class II | Active |
| Sofsilk | S-405 | FDA UDI | Class II | Active |
| Mon-a-Therm | 502-0400A | FDA UDI | Class II | Active |
| Fortrex | A35HPV04100135 | FDA UDI | Class II | Active |
| Valtrac | 8886808400 | FDA UDI | Class II | Unknown |
| Syneture | US1438 | FDA UDI | Class II | Unknown |
| Polysorb | L-1670-K | FDA UDI | Class II | Active |
| Polysorb | CLS-884 | FDA UDI | Class II | Unknown |
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. |