Identity
- Trade Name
- ViperTrack FDA UDI
- Generic Name
- X-ray film ruler FDA UDI
- Device Name
- VIPERTRACK, 20 PACK FDA UDI
- Model / Reference
- VPR-TRK 20 FDA UDI
- Description
- VIPERTRACK, 20 PACK FDA UDI
Identifiers
- Catalog Number
- 72014-01 FDA UDI
- Primary DI / UDI-DI
- 10852528005091 FDA UDI
- FDA Product Code
- FTY FDA UDI
- GMDN Term
- X-ray film ruler FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Ethylene Oxide FDA UDI
Dimensions & Sizes
- Size
- Length — 30 Centimeter FDA UDI
Category: X-ray film ruler
ViperTrack by Cardiovascular Systems, Inc. — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Cardiovascular Systems, Inc.
Sources (1)
- FDA UDI ea5faa28-a458-40a0-980a-e0aec2f2f5f7 36 fields · synced May 30, 2026