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ViperWire

FDA UDI

Class II (US FDA UDI)

by Cardiovascular Systems, Inc.

Identity

Trade Name
ViperWire FDA UDI
Generic Name
Peripheral vascular guidewire, manual FDA UDI
Device Name
VIPERWIRE, ADVANCED, .012" DIA .012" SPRING TIP, 200CM, 5 PACK FDA UDI
Model / Reference
VPR-GW-200 FDA UDI
Description
VIPERWIRE, ADVANCED, .012" DIA .012" SPRING TIP, 200CM, 5 PACK FDA UDI

Identifiers

Catalog Number
7-10004 FDA UDI
Primary DI / UDI-DI
10852528005220 FDA UDI
FDA Product Code
MCW FDA UDI
GMDN Term
Peripheral vascular guidewire, manual FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4875 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
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Length — 200 Centimeter FDA UDI

Category: Peripheral vascular guidewire, manual

ViperWire by Cardiovascular Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral vascular guidewire, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardiovascular Systems, Inc.

Sources (1)

  • FDA UDI 782c56b9-bb26-4a5f-a48c-4fc828810b0c 36 fields · synced May 30, 2026