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RadiStop™

FDA UDI

Class I (US FDA UDI)

by St. Jude Medical, Inc.

Identity

Trade Name
RadiStop™ FDA UDI
Generic Name
Radial artery compression device FDA UDI
Device Name
Compression Assist Device FDA UDI
Model / Reference
C11177 FDA UDI
Description
Compression Assist Device FDA UDI

Identifiers

Catalog Number
C11177 FDA UDI
Primary DI / UDI-DI
05414734050050 FDA UDI
FDA Product Code
GAX FDA UDI
GMDN Term
Radial artery compression device FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.5900 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

Yes

FDA UDI

Category: Radial artery compression device

RadiStop™ by St. Jude Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radial artery compression device.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI de449ba9-3dfc-4721-a7f3-272324e655ee 36 fields · synced May 30, 2026