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Results for “Vascular procedure pack”

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Registry EUDAMED 17 FDA 510(k) 1 FDA PMA GUDID 8

Country / market United States 9

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Türkiye 1

Risk class Class I 4 Class IIa Class IIb 16 Class III 2 Class II (US) 4

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Class A Class B Class C Class D IVD General IVD Annex II List A IVD Annex II List B IVD for self-testing Active implantable (AIMDD) Unclassified (FDA) Not classified (FDA)

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26 devices foundsorted by relevance

Device · Manufacturer · Authorizations

VSI Radiofrequency Ablation Procedure Pack with 7F 7cm Introducer Kit 7788

Vascular Solutions, Inc.,United States Class I

Withdrawn GUDID I
VSI Radiofrequency Ablation Procedure Pack with 7F 12cm Micro-HV Kit 7797

Vascular Solutions, Inc.,United States Class II

Withdrawn GUDID II
VSI Basic Radiofrequency Ablation Procedure Pack with 7F 11cm Introducer Kit 7787

Vascular Solutions, Inc.,United States Class I

Withdrawn GUDID I
VSI Radiofrequency Ablation Procedure Pack with 7F 11cm Introducer Kit 7789

Vascular Solutions, Inc.,United States Class II

Withdrawn GUDID II
VSI Radiofrequency Ablation Procedure Pack with 7F 7cm Micro-HV Kit 7796

Vascular Solutions, Inc.,United States Class II

Withdrawn GUDID II
PeritX™ 1L Drainage Kit (90-1010); PeritX™ 2L Drainage Kit (90-2010); PeritX™ Peritoneal Catheter Kit (50-9000C); PeritX™ Peritoneal Catheter and Starter Kit (50-9900C); PeritX™ Peritoneal Catheter Mini Kit (50-9050A); PleurX™ Low Profile Catheter Mini Kit (50-8050); Valve Cap (50-7235A); PeritX™ Valve Kit (50-7272); Catheter Access Kit (50-7280A); Lockable Drainage Line (50-7245A); Lockable Drainage Line Kit (50-7265A); PleurX™ Supplemental Insertion Kit (50-7262); Procedure Pack (50-

Bard Peripheral Vascular, Inc.,United States(FDA 510(k) applicant) Class II

Active 510(k) 510(k) II

Showing 21-26 of 26

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