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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 31 of 194

Device	Model / Reference	Registries	Class	Status
Polysorb	UL-202	FDA UDI	Class II	Active
The BigEasy	MVA100	FDA UDI	Class II	Active
Endo Clip	176502	FDA UDI	Class II	Unknown
V-Loc 90	VLOCM0344	FDA UDI	Class II	Active
Syneture	US1548	FDA UDI	Class II	Unknown
Polysorb	CL6G	FDA UDI	Class II	Unknown
Shiley	4CN65A	FDA UDI	Class II	Active
Plain Gut	SG-5654	FDA UDI	Class II	Active
Chromic Gut	G-83	FDA UDI	Class II	Unknown
Plain Gut	CG-873	FDA UDI	Class II	Unknown
Surgipro ll	SP-5663	FDA UDI	Class II	Active
Shiley	6.0 PDL	FDA UDI	Class II	Active
Chromic Gut	3-CG-802	FDA UDI	Class II	Unknown
Surgipro II	XX-5247	FDA UDI	Class II	Active
Step	S100700	FDA UDI	Class II	Active
Lapro-Clip	8886848798	FDA UDI	Class II	Active
Shiley	125132	FDA UDI	Class II	Active
Polysorb	170054	FDA UDI	Class II	Active
Biosyn	M-33	FDA UDI	Class II	Active
Monosof	SN-665	FDA UDI	Class II	Active
Polysorb	CL-14-MG	FDA UDI	Class II	Active
Shiley	86267	FDA UDI	Class II	Active
Vital Sync	VITALSYNCSW03	FDA UDI	Class II	Active
Mallinckrodt	86643	FDA UDI	Class II	Unknown
Nellcor	P-000265-00	FDA UDI	Class II	Unknown
Surgipro ll	VP-841-X	FDA UDI	Class II	Active
Monosof	N-63	FDA UDI	Class II	Active
Bluntport Plus	179075P	FDA UDI	Class II	Active
Plain Gut	SG-751	FDA UDI	Class II	Active
TrailBlazer™ Angled	ASC-018-150	FDA UDI	Class II	Active
Surgipro II	SP5697GMDL	FDA UDI	Class II	Unknown
Vital Sync	EWSSW01	FDA UDI	N/A	Active
Syneture	US1670	FDA UDI	Class II	Unknown
Syneture	US1551	FDA UDI	Class II	Unknown
Surgipro II	VP-831-X	FDA UDI	Class II	Active
Surgilon	88861931-33	FDA UDI	Class II	Unknown
Surgipro ll	VP-904-X	FDA UDI	Class II	Active
Valleylab	E2100E	FDA UDI	Class II	Active
Biosyn	M-115	FDA UDI	Class II	Unknown
Dar	R023	FDA UDI	Class II	Unknown
RapidCross™	A14BX035020090	FDA UDI	Class II	Active
Syneture	US1487	FDA UDI	Class II	Unknown
Sofsilk	VS-871	FDA UDI	Class II	Active
Syneture	US0285	FDA UDI	Class II	Unknown
Ti-Cron	88863324-56	FDA UDI	Class II	Active
Chromic Gut	CG-415	FDA UDI	Class II	Active
Protege GPS	SERB65-09-40-120	FDA UDI	Class II	Active
Sils	SILSCLINCH46	FDA UDI	Class II	Unknown
Biosyn	CMT-950-M	FDA UDI	Class II	Active
Polysorb	XX-5231	FDA UDI	Class II	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.