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Rad-Sure™

FDA UDI

Class I (US FDA UDI)

by Ashland Specialty Ingredients, G.P.

Identity

Trade Name
Rad-Sure™ FDA UDI
Generic Name
Device operating status label/tag, single-use FDA UDI
Device Name
Blood Irradiation Indicator FDA UDI
Model / Reference
15 Gy Sample @24SH (consolidated XR/G) FDA UDI
Description
Blood Irradiation Indicator FDA UDI

Identifiers

Catalog Number
980690 FDA UDI
Primary DI / UDI-DI
00810106410326 FDA UDI
FDA Product Code
KSS FDA UDI
GMDN Term
Device operating status label/tag, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.9050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Category: Device operating status label/tag, single-use

Rad-Sure™ by Ashland Specialty Ingredients, G.P. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Device operating status label/tag, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 036c98e5-278e-4fbf-af07-00e32389e138 34 fields · synced Jun 9, 2026