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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 26 of 194

Device	Model / Reference	Registries	Class	Status
EndoFLIP	EF-100	FDA UDI	Class II	Active
Surgilon	88861985-51	FDA UDI	Class II	Active
Dar	444SP01014	FDA UDI	Class I	Active
Ti-Cron	VCD2031MSE	FDA UDI	Class II	Active
Tri-Staple 2.0	SIGC60V	FDA UDI	Class II	Unknown
Steel	W-22G	FDA UDI	Class II	Unknown
HawkOne™	H1-S	FDA UDI	Class II	Active
Mallinckrodt	86199	FDA UDI	Class II	Active
Mallinckrodt	86525	FDA UDI	Class II	Unknown
Sofsilk	170003	FDA UDI	Class II	Active
Surgipro ll	VP-903-MX	FDA UDI	Class II	Active
Surgipro ll	VP-726-X	FDA UDI	Class II	Active
RapidCross™	A14BX025210170	FDA UDI	Class II	Active
Fortrex™	A35HPV08040080	FDA UDI	Class II	Active
Signia	SIGCIRADAPTXL	FDA UDI	Class II	Unknown
Mallinckrodt	96111	FDA UDI	Class II	Unknown
Shiley	10FENJ-S	FDA UDI	Class II	Active
Ti-Cron	XX-5179	FDA UDI	Class II	Unknown
Chromic Gut	SG-197	FDA UDI	Class II	Active
Chromic Gut	CG-815	FDA UDI	Class II	Active
Valleylab	E1552-6	FDA UDI	Class II	Active
ClosureFast	CFP	FDA UDI	Class II	Active
Chemosite	120112	FDA UDI	Class II	Unknown
Surgidac	D-1764	FDA UDI	Class II	Unknown
RapidCross™	A14BX035080170	FDA UDI	Class II	Active
Mon-a-Therm	90044	FDA UDI	Class II	Active
Biosyn	UM-345	FDA UDI	Class II	Active
Surgipro ll	X-1157	FDA UDI	Class II	Active
Shiley	8FENJ	FDA UDI	Class II	Active
Chromic Gut	SG-535	FDA UDI	Class II	Active
Ti-Cron	X1383	FDA UDI	Class II	Unknown
Syneture	US1378	FDA UDI	Class II	Unknown
Puritan Bennett	10049985	FDA UDI	Class II	Unknown
Dar	444SPA0000	FDA UDI	Class I	Active
Mallinckrodt	18775	FDA UDI	Class II	Active
Pi	4907T	FDA UDI	Class II	Unknown
Surgipro	X1374	FDA UDI	Class II	Unknown
Puritan Bennett	10086048	FDA UDI	Class II	Active
Monosof	CN-792	FDA UDI	Class II	Active
Monosof	XX-5198	FDA UDI	Class II	Unknown
V-Loc	VLOCN208L	FDA UDI	Class II	Active
iDrive Ultra	IDRVULTRA2	FDA UDI	Class II	Active
Polysorb	CL-953	FDA UDI	Class II	Active
Surgipro	CP-836	FDA UDI	Class II	Active
Fortrex™	A35HPV10040135	FDA UDI	Class II	Active
Surgipro ll	VPP-557-X	FDA UDI	Class II	Active
Ti-Cron	88863103-71	FDA UDI	Class II	Active
OptiMumm	E3635	FDA UDI	Class II	Unknown
Nellcor	PMSW-RR-V2.0	FDA UDI	Class II	Active
Polysorb	CL-375-MG	FDA UDI	Class II	Active

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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.