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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 3 of 194| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Monosof | SN-368 | FDA UDI | Class II | Active |
| Signia | SIGSDS30CTV | FDA UDI | Class II | Active |
| Shiley | 18885S | FDA UDI | Class II | Active |
| Shiley | M5.5PLC | FDA UDI | Class II | Active |
| Gia | GIA60MTC | FDA UDI | Class II | Active |
| Mallinckrodt | 86466 | FDA UDI | Class II | Unknown |
| Sofsilk | SS-685 | FDA UDI | Class II | Active |
| Mallinckrodt | 86521 | FDA UDI | Class II | Active |
| Syneture | US1602 | FDA UDI | Class II | Unknown |
| VersaOne | RC8LGS | FDA UDI | Class II | Active |
| Valleylab | E1510 | FDA UDI | Class II | Active |
| Maxon CV | 8886 6148-11 | FDA UDI | Class II | Unknown |
| Mallinckrodt | 86080 | FDA UDI | Class II | Unknown |
| SpiderFX | SPD2-US-050-190 | FDA UDI | Class II | Active |
| Valleylab | E1020 | FDA UDI | Class II | Active |
| Puritan Bennett | 980X3SLDRAC | FDA UDI | Class II | Active |
| Sgia | SGIA6038S | FDA UDI | Class II | Active |
| Puritan Bennett | 980X3ENDRAC | FDA UDI | Class II | Active |
| Endo Mini-Shears | 174309 | FDA UDI | Class II | Active |
| Shiley | 6CN75R | FDA UDI | Class II | Active |
| ClosureRFG | RFG2 | FDA UDI | Class II | Active |
| Nellcor | FLEXMAX | FDA UDI | Class II | Active |
| Invos | RSC-3 | FDA UDI | Class II | Active |
| Puritan Bennett | 4-070305-00 | FDA UDI | Class II | Active |
| EverCross | AB35W05020135 | FDA UDI | Class II | Active |
| Caprosyn | CC-912 | FDA UDI | Class II | Active |
| Ti-Cron | 88863229-41 | FDA UDI | Class II | Active |
| Polysorb | L-1590-K | FDA UDI | Class II | Unknown |
| Steel | 88862382-83 | FDA UDI | Class II | Active |
| Monosof | X-1127L | FDA UDI | Class II | Unknown |
| Chromic Gut | CG-801 | FDA UDI | Class II | Unknown |
| Shiley | 109865 | FDA UDI | Class II | Active |
| Caprosyn | GC-225 | FDA UDI | Class II | Unknown |
| Biosyn | CM-208 | FDA UDI | Class II | Active |
| RapidCross™ | A14BX030210170 | FDA UDI | Class II | Active |
| Sofsilk | VS81G | FDA UDI | Class II | Active |
| V-Loc | VLOCN204L | FDA UDI | Class II | Active |
| EverCross | AB35W04020135 | FDA UDI | Class II | Active |
| Nitrex™ | N352601 | FDA UDI | Class II | Active |
| Endo GIA | 030453 | FDA UDI | Class II | Active |
| Velosorb Fast | SV-6840 | FDA UDI | Class II | Active |
| Mallinckrodt | 96595 | FDA UDI | Class II | Unknown |
| Ti-Cron | 88863160-41 | FDA UDI | Class II | Active |
| Ti-Cron | 88863008-51 | FDA UDI | Class II | Active |
| Laparofan | OMSLF10 | FDA UDI | Class II | Unknown |
| Mallinckrodt | 86213 | FDA UDI | Class II | Unknown |
| Syneture | US1703 | FDA UDI | Class II | Unknown |
| Syneture | US1353 | FDA UDI | Class II | Unknown |
| Monosof | SN-367 | FDA UDI | Class II | Active |
| Valleylab | E2516HGNSB | FDA UDI | Class II | Active |
Related Companies
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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. |