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SecureShield© Multipurpose with fenestration 12" x 17" Scatter Reducing Drape

FDA UDI

Class I (US FDA UDI)

by Barrier Technologies, Llc

Identity

Trade Name
SecureShield© Multipurpose with fenestration 12" x 17" Scatter Reducing Drape FDA UDI
Generic Name
Patient radiation shielding pad/drape, single-use FDA UDI
Device Name
Outstanding protection during all types of biopsy procedures. Rectangular fenestration allows access and viewing while minimizing radiation exposure. The SecureShield Biopsy Shield provides excellent protection during any needle biopsy or puncture procedure. This versatile shield can be effectively used at any location on the body. FDA UDI
Model / Reference
SS-5200 FDA UDI
Description
Outstanding protection during all types of biopsy procedures. Rectangular fenestration allows access and viewing while minimizing radiation exposure. The SecureShield Biopsy Shield provides excellent protection during any needle biopsy or puncture procedure. This versatile shield can be effectively used at any location on the body. FDA UDI

Identifiers

Primary DI / UDI-DI
10860004894633 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 with fenestration 12" x 17" 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 e6490dcf-6188-416f-a474-a14f226d26a4 33 fields · synced May 29, 2026