Identity
- Trade Name
- VSI FDA UDI
- Generic Name
- Varicose vein lasing procedure kit FDA UDI
- Device Name
- Vascular Solutions Custom Access Kit FDA UDI
- Model / Reference
- IPN001695 FDA UDI
- Description
- Vascular Solutions Custom Access Kit FDA UDI
Identifiers
- Catalog Number
- 7717 FDA UDI
- Primary DI / UDI-DI
- 10841156106201 FDA UDI
- FDA Product Code
- GEX FDA UDI
- GMDN Term
- Varicose vein lasing procedure kit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4810 FDA UDI
- Commercial Distribution
- 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
Dimensions & Sizes
- Size
- Needle Gauge — 21 Gauge FDA UDILength — 70 Centimeter FDA UDI
Category: Varicose vein lasing procedure kit
Vsi by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Teleflex Incorporated
Sources (1)
- FDA UDI 96a16795-26b9-43fe-ac4d-872bffab10fb 36 fields · synced May 31, 2026