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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 14 of 194

Device	Model / Reference	Registries	Class	Status
Shiley	87460	FDA UDI	Class II	Active
Mon-a-Therm	502-0400A	FDA UDI	Class II	Active
Shiley	10UN10H	FDA UDI	Class II	Active
Shiley	86201	FDA UDI	Class II	Active
Sofsilk	GSJ-47-M	FDA UDI	Class II	Unknown
Monosof	SN-5662G	FDA UDI	Class II	Active
Ti-Cron	XX-5034	FDA UDI	Class II	Unknown
Monosof	N-2810	FDA UDI	Class II	Unknown
Mon-a-Therm	90051	FDA UDI	Class II	Active
Puritan Bennett	10049998-RFB	FDA UDI	Class II	Active
Sofsilk	SS-5640G	FDA UDI	Class II	Unknown
Shiley	M3.0PED	FDA UDI	Class II	Active
Shiley	18875	FDA UDI	Class II	Active
Versaport Plus	179102P	FDA UDI	Class II	Active
Sofsilk	GS-44-M	FDA UDI	Class II	Active
Surgipro II	VP-745-X	FDA UDI	Class II	Active
Force FX	Force FX-C ZD	FDA UDI	Class II	Unknown
Surgilon	88861968-51	FDA UDI	Class II	Unknown
Polysorb	X-1045	FDA UDI	Class II	Unknown
Surgipro II	VP-727-X	FDA UDI	Class II	Active
Dar	351/5410Z	FDA UDI	Class II	Active
Maxon	XX2211	FDA UDI	Class II	Active
Puritan Bennett	S-232102-00B	FDA UDI	Class I	Unknown
Valleylab	E0510	FDA UDI	Class II	Active
PowerCross	AB18W020200090	FDA UDI	Class II	Active
Ta 90 Bn	010885	FDA UDI	Class I	Unknown
Maxon CV	8886 6139-01	FDA UDI	Class II	Unknown
Polysorb	GL-226	FDA UDI	Class II	Active
Mini Port	171315	FDA UDI	Class II	Unknown
Puritan Bennett	4-840220DIEC-RS	FDA UDI	Class II	Unknown
Mallinckrodt	86652	FDA UDI	Class II	Unknown
Dar	444SP01116	FDA UDI	Class I	Active
Biosyn	CM-767L	FDA UDI	Class II	Active
Dar	444SP03012	FDA UDI	Class I	Active
Tri-Staple 2.0	SIGCIR31XT	FDA UDI	Class II	Active
Biosyn	CM-126	FDA UDI	Class II	Active
Visi-Pro™	PXB35-06-37-135	FDA UDI	Class III	Active
Dar	444SP02312	FDA UDI	Class I	Active
LigaSure	LIGASUREZD	FDA UDI	Class II	Active
Biosyn	XX-5244	FDA UDI	Class II	Unknown
Puritan Bennett	10049981	FDA UDI	Class II	Unknown
Ti-Cron	X1373	FDA UDI	Class II	Unknown
superDimension	AAS00161-20	FDA UDI	Class II	Active
Nellcor	DSPM10N	FDA UDI	Class II	Active
Spacemaker	VBD240T	FDA UDI	Class II	Unknown
Polysorb	L-4	FDA UDI	Class II	Active
Ti-Cron	88863226-41	FDA UDI	Class II	Active
Shiley	4.0NEF-P	FDA UDI	Class II	Unknown
Syneture	US1026A	FDA UDI	Class II	Unknown
LigaSure Advance	LF5544	FDA UDI	Class II	Active

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Importers

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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.