Identity
- Trade Name
- VARI-LASE FDA UDI
- Generic Name
- Varicose vein lasing procedure kit FDA UDI
- Device Name
- Vari-Lase Kit 4F 24cm PT Bright 21G FDA UDI
- Model / Reference
- IPN913596 FDA UDI
- Description
- Vari-Lase Kit 4F 24cm PT Bright 21G FDA UDI
Identifiers
- Catalog Number
- 7170 FDA UDI
- Primary DI / UDI-DI
- 10841156100988 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
- Catheter Gauge — 4 French FDA UDILength — 250 Centimeter FDA UDI
Category: Varicose vein lasing procedure kit
Vari-Lase 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 31d64506-cfaa-4dd1-a01a-8649aca30e32 36 fields · synced Jun 8, 2026