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Rad Control

FDA UDI

Class I (US FDA UDI)

by Typenex Medical, LLC

Identity

Trade Name
Rad Control FDA UDI
Generic Name
Blood irradiation indicator FDA UDI
Device Name
15 Gy Universal Irradiation Tag FDA UDI
Model / Reference
RT0302 FDA UDI
Description
15 Gy Universal Irradiation Tag FDA UDI

Identifiers

Primary DI / UDI-DI
00810050855457 FDA UDI
FDA Product Code
IWZ FDA UDI
GMDN Term
Blood irradiation indicator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.1840 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: Blood irradiation indicator

Rad Control by Typenex Medical, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood irradiation indicator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7dbbf966-0d37-41b9-b027-8ba24ead77a4 33 fields · synced May 31, 2026