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Covidien LP

Last updated May 24, 2026

Information

Country: US
Address: —
Website: covidien.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +1(508)261-8000
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: 058614483

Catalogue (9686)

Page 12 of 194

Device	Model / Reference	Registries	Class	Status
Sofsilk	CS-562	FDA UDI	Class II	Active
Monosof	SN-658	FDA UDI	Class II	Active
Puritan Bennett	4-840120DICU-FR	FDA UDI	Class II	Unknown
Chemosite	120035	FDA UDI	Class II	Unknown
Ti-Cron	X-1186	FDA UDI	Class II	Unknown
EverFlex™	EVD35-07-020-120	FDA UDI	Class III	Active
RapidCross	A14BX035210090	FDA UDI	Class II	Active
Syneture	US1662	FDA UDI	Class II	Unknown
Shiley	86466	FDA UDI	Class II	Unknown
Caprosyn	CC-915	FDA UDI	Class II	Active
Shiley	86224	FDA UDI	Class II	Unknown
Shiley	M0PT	FDA UDI	Class II	Active
Dar	330/5109	FDA UDI	Class I	Active
V-Loc 180	VLOCL2826	FDA UDI	Class II	Active
Syneture	US1064	FDA UDI	Class II	Unknown
Mallinckrodt	86271	FDA UDI	Class II	Unknown
Syneture	US1688	FDA UDI	Class II	Unknown
Syneture	US1615	FDA UDI	Class II	Unknown
Multifire Premium	059036	FDA UDI	Class I	Active
Surgipro II	VP-735-MX	FDA UDI	Class II	Active
Surgipro ll	VPF-720-X	FDA UDI	Class II	Active
Fortrex™	A35HPV04040080	FDA UDI	Class II	Active
Shiley	96565	FDA UDI	Class II	Unknown
Mallinckrodt	76285	FDA UDI	Class II	Active
Chromic Gut	CG-943	FDA UDI	Class II	Unknown
Syneture	US1380	FDA UDI	Class II	Unknown
Surgipro	XX-5069	FDA UDI	Class II	Unknown
Surgilon	88861951-71	FDA UDI	Class II	Unknown
Biosyn	CM-30-M	FDA UDI	Class II	Active
Mallinckrodt	109890	FDA UDI	Class II	Active
Maxon	8886 6285-51	FDA UDI	Class II	Unknown
Velosorb Fast	SV-2296	FDA UDI	Class II	Active
Gia	GIA80XTS	FDA UDI	Class II	Active
Barrx	CYTO-KIT-USM	FDA UDI	Class I	Active
Sofsilk	SS-5678	FDA UDI	Class II	Active
Wholey™	WWSS35260	FDA UDI	Class II	Active
Dar	352/5877TC	FDA UDI	Class II	Active
TrailBlazer™ Angled	ASC-035-135	FDA UDI	Class II	Active
Dar	444SPY1316	FDA UDI	Class I	Active
Puritan Bennett	10051470	FDA UDI	Class II	Unknown
Nellcor	MAXFAST	FDA UDI	Class II	Active
Chemosite	120023A	FDA UDI	Class II	Unknown
Valleylab	E3783-28	FDA UDI	Class II	Active
Sofsilk	S-204	FDA UDI	Class II	Unknown
Reliamax	GIA80RS	FDA UDI	Class II	Active
Puritan Bennett	4-840120DICU-EN	FDA UDI	Class II	Unknown
Puritan Bennett	980U3ESDIUU	FDA UDI	Class II	Unknown
Valleylab	E7512	FDA UDI	Class II	Active
Surgipro ll	VPF-522-X	FDA UDI	Class II	Active
McGRATH MAC	350-086-000	FDA UDI	Class I	Active

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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.