Identity
- Trade Name
- Viperslide FDA UDI
- Generic Name
- Atherectomy system lubricant FDA UDI
- Device Name
- VIPERSLIDE, 100ML BAG, 10 PK FDA UDI
- Model / Reference
- VPR-SLD2 FDA UDI
- Description
- VIPERSLIDE, 100ML BAG, 10 PK FDA UDI
Identifiers
- Catalog Number
- 72031-01 FDA UDI
- Primary DI / UDI-DI
- 10852528005121 FDA UDI
- FDA Product Code
- MCX FDA UDI
- GMDN Term
- Atherectomy system lubricant FDA UDI
Classification
- Device Class
- Class III 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
No
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
Moist Heat or Steam Sterilization FDA UDI
Category: Atherectomy system lubricant
Viperslide by Cardiovascular Systems, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 III | Pending data |
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Manufacturer
- Manufacturer
- Cardiovascular Systems, Inc.
Sources (1)
- FDA UDI 38b3a3f1-a891-44a1-b1d0-48ac2d4255fb 36 fields · synced Jun 8, 2026