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ViperTrack

FDA UDI

Class I (US FDA UDI)

by Cardiovascular Systems, Inc.

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
Sterilization Method
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

Similar devices

Also classified as X-ray film ruler.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ea5faa28-a458-40a0-980a-e0aec2f2f5f7 36 fields · synced May 30, 2026