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Rayshield

FDA UDI

Class I (US FDA UDI)

by Aadco Medical, Inc.

Identity

Trade Name
Rayshield FDA UDI
Generic Name
Patient radiation shielding pad/drape, reusable FDA UDI
Device Name
PEDIATRIC GONAD SHIELD SET FDA UDI
Model / Reference
LP-040 FDA UDI
Description
PEDIATRIC GONAD SHIELD SET FDA UDI

Identifiers

Catalog Number
LP-040 FDA UDI
Primary DI / UDI-DI
00840348529265 FDA UDI
FDA Product Code
IWT FDA UDI
GMDN Term
Patient radiation shielding pad/drape, reusable 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

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Patient radiation shielding pad/drape, reusable

Rayshield by Aadco Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient radiation shielding pad/drape, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aadco Medical, Inc.

Sources (1)

  • FDA UDI d3d066a5-33cf-46e2-a607-69c7052a1bf2 34 fields · synced May 30, 2026