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Radpad

FDA UDI

Class I (US FDA UDI)

by Worldwide Innovations & Technologies, Inc.

Identity

Trade Name
RADPAD FDA UDI
Generic Name
Radiation shielding blanket FDA UDI
Device Name
Diagnostic Shield-Yellow FDA UDI
Model / Reference
5901A-Y FDA UDI
Description
Diagnostic Shield-Yellow FDA UDI

Identifiers

Primary DI / UDI-DI
00852814003834 FDA UDI
FDA Product Code
KPY FDA UDI
GMDN Term
Radiation shielding blanket FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.6500 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Radiation shielding blanket

Radpad by Worldwide Innovations & Technologies, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiation shielding blanket.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Worldwide Innovations & Technologies, Inc.

Sources (1)

  • FDA UDI 5b80e2d4-32ec-4197-9a8b-05566b721df8 33 fields · synced Jun 9, 2026