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VSI Radiofrequency Ablation Procedure Pack with 7F 11cm Introducer Kit
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- VSI Radiofrequency Ablation Procedure Pack with 7F 11cm Introducer Kit FDA UDI
- Generic Name
- General surgical procedure kit, non-medicated, single-use FDA UDI
- Model / Reference
- 7789 FDA UDI
Identifiers
- Primary DI / UDI-DI
- M20677890 FDA UDI
- FDA Product Code
- LRO FDA UDILRP FDA UDI
- GMDN Term
- General surgical procedure kit, non-medicated, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4370 FDA UDI878.4800 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
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 11cm Introducer Kit by Vascular Solutions, Inc. — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Vascular Solutions, Inc.
Sources (1)
- FDA UDI d249bab7-9b9b-4e18-91ea-bb8fa944caa7 34 fields · synced Jun 8, 2026