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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 20 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Puritan Bennett | 980N1ENDIUU-LA | FDA UDI | Class II | Unknown |
| Biosyn | CM-765-L | FDA UDI | Class II | Active |
| Puritan Bennett | 10084332 | FDA UDI | Class II | Active |
| Ta | TA6035L | FDA UDI | Class II | Active |
| Biosyn | UM-243 | FDA UDI | Class II | Active |
| Mini Shears | 171305 | FDA UDI | Class II | Unknown |
| Vascufil | 88864726-41V | FDA UDI | Class II | Unknown |
| RapidCross | A14BX020120170 | FDA UDI | Class II | Active |
| ClosureRFS | RFS2-6-12 | FDA UDI | Class II | Active |
| Edge | E1450XNSB | FDA UDI | Class II | Active |
| Barrx | GW-002B | FDA UDI | Class II | Active |
| Monosof | SN-669 | FDA UDI | Class II | Active |
| Monosof | SN-5670 | FDA UDI | Class II | Active |
| Vascufil | 88864739-21V | FDA UDI | Class II | Unknown |
| IntraStent LD Max | S18-26 | FDA UDI | Class II | Active |
| PTFE Polymer Pledgets | VPG56FE | FDA UDI | Class II | Active |
| Puritan Bennett | 4-074601-00 | FDA UDI | Class II | Active |
| EverFlex™ | EVD35-06-150-080 | FDA UDI | Class III | Active |
| Novafil | 8886 4414-31 | FDA UDI | Class II | Active |
| Surgilon | 88861995-41 | FDA UDI | Class II | Active |
| Surgipro ll | VP-870-X | FDA UDI | Class II | Active |
| Shiley | 85590 | FDA UDI | Class II | Active |
| Ila | 3973 | FDA UDI | Class II | Unknown |
| Ti-Cron | XX-5090 | FDA UDI | Class II | Unknown |
| Vascufil | 88864719-21V | FDA UDI | Class II | Unknown |
| Ti-Cron | 88863109-43 | FDA UDI | Class II | Active |
| EverCross | AB35W09040135 | FDA UDI | Class II | Active |
| Shiley | M8DCFN | FDA UDI | Class II | Active |
| Arcpoint | ILS-1800-PN | FDA UDI | Class II | Active |
| Sofsilk | SS-621 | FDA UDI | Class II | Active |
| Shiley | 33760 | FDA UDI | Class I | Active |
| Fortrex | A35HPV08080135 | FDA UDI | Class II | Active |
| Surgiwand II | 178081 | FDA UDI | Class II | Active |
| Syneture | US1395 | FDA UDI | Class II | Unknown |
| Surgipro II | X-1307 | FDA UDI | Class II | Active |
| RapidCross™ | A14BX030210090 | FDA UDI | Class II | Active |
| Endo GIA | EGIA45CTAV | FDA UDI | Class II | Active |
| Maxon | 8886 6269-61 | FDA UDI | Class II | Active |
| Nellcor | MC10 | FDA UDI | Class II | Active |
| Maxon | 8886 6219-33 | FDA UDI | Class II | Active |
| V-Loc 180 | VLOCL0643 | FDA UDI | Class II | Active |
| Nitrex | N183001 | FDA UDI | Class II | Active |
| Syneture | US1388 | FDA UDI | Class II | Unknown |
| Shiley | 86284 | FDA UDI | Class II | Unknown |
| Fortrex™ | A35HPV08040135 | FDA UDI | Class II | Active |
| Kangaroo | 8884721088 | FDA UDI | Class II | Active |
| Nellcor | DLN560 | FDA UDI | Class II | Active |
| Syneture | US1719 | FDA UDI | Class II | Unknown |
| Novafil | 8886 4402-33 | FDA UDI | Class II | Active |
| EverFlex | PRB35-06-030-080 | FDA UDI | Class III | 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. |