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Radpad

FDA UDI

Class II (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
Verterbro/Kyphoplasty Drape - Yellow FDA UDI
Model / Reference
7400-Y FDA UDI
Description
Verterbro/Kyphoplasty Drape - Yellow FDA UDI

Identifiers

Primary DI / UDI-DI
00852814003223 FDA UDI
FDA Product Code
PUI FDA UDI
GMDN Term
Patient radiation shielding pad/drape, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 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: Patient radiation shielding pad/drape, single-use

Radpad by Worldwide Innovations & Technologies, Inc. — Class II — 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 26755eaa-d34f-48cb-9c54-f7747894dce4 33 fields · synced Jun 9, 2026