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VSI Radiofrequency Ablation Procedure Pack with 7F 7cm Introducer Kit
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- VSI 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
- 7788 FDA UDI
Identifiers
- Primary DI / UDI-DI
- M20677880 FDA UDI
- FDA Product Code
- LRP FDA UDILRO 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 UDI878.4370 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
VSI 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Vascular Solutions, Inc.
Sources (1)
- FDA UDI f5be13fd-e576-4e37-b17b-b47ea5db46a9 34 fields · synced May 30, 2026