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SecureShield© Multipurpose 12" x 36" Scatter Reducing Drape

FDA UDI

Class I (US FDA UDI)

by Barrier Technologies, Llc

Identity

Trade Name
SecureShield© Multipurpose 12" x 36" Scatter Reducing Drape FDA UDI
Generic Name
Patient radiation shielding pad/drape, single-use FDA UDI
Device Name
Multi-purpose shield provides excellent protection during many types of procedures. Provides a comprehensive zone of protection for the head, hands and body of the entire team. FDA UDI
Model / Reference
SS-5100-XL FDA UDI
Description
Multi-purpose shield provides excellent protection during many types of procedures. Provides a comprehensive zone of protection for the head, hands and body of the entire team. FDA UDI

Identifiers

Primary DI / UDI-DI
10860004894671 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

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

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

SecureShield© Multipurpose 12" x 36" Scatter Reducing Drape by Barrier Technologies, Llc — Class I — FDA UDI — listed in FDA GUDID

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

Sources (1)

  • FDA UDI a7f68d5f-2267-4690-83cb-09a23ab8da09 33 fields · synced May 30, 2026