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

FDA UDI

Class I (US FDA UDI)

by Vascular Solutions, Inc.

Identity

Trade Name
VSI Basic Radiofrequency Ablation Procedure Pack with 7F 7cm Introducer Kit FDA UDI
Generic Name
General surgical procedure kit, non-medicated, single-use FDA UDI
Model / Reference
7786 FDA UDI

Identifiers

Primary DI / UDI-DI
M20677860 FDA UDI
FDA Product Code
LRP FDA UDI
GMDN Term
General surgical procedure kit, non-medicated, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

VSI Basic Radiofrequency Ablation Procedure Pack with 7F 7cm Introducer Kit by Vascular Solutions, Inc. — Class I — FDA UDI — listed in FDA GUDID

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vascular Solutions, Inc.

Sources (1)

  • FDA UDI 6e474960-da53-4ac1-bb0f-a69cb681144c 34 fields · synced Jun 1, 2026