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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
Patient radiation shielding pad/drape, single-use FDA UDI
Device Name
Fenestrated Radial Shield Bulk Non-Sterile - Orange FDA UDI
Model / Reference
5511A-O-Bulk-NS FDA UDI
Description
Fenestrated Radial Shield Bulk Non-Sterile - Orange FDA UDI

Identifiers

Primary DI / UDI-DI
00852814003926 FDA UDI
FDA Product Code
KPY FDA UDI
GMDN Term
Patient radiation shielding pad/drape, single-use 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Patient radiation shielding pad/drape, single-use

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

Similar devices

Also classified as Patient radiation shielding pad/drape, single-use.

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 860883fc-a5f6-4253-af0e-df3f544c5680 33 fields · synced Jun 9, 2026