AccessGUDID - DEVICE: SecureShield© for Dialysis 42" x 32" Scatter Reducing Drape (10860004894664)

GUDID

Device Identifier (DI) Information

Brand Name: SecureShield© for Dialysis 42" x 32" Scatter Reducing Drape
Version or Model: SS-7200
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: Barrier Technologies, LLC

Primary DI Number: 10860004894664
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 621134084 *Terms of Use

Device Description: Outstanding protection during dialysis declotting procedures. Up to 80+% and 50% exposure reductions at hands and eyes, respectively. Shielding is easily adjustable as needed. Clinically proven to attenuate 95% of a 100kV direct beam. SecureShield Dialysis Access pads provide excellent protection for interventionalists and their teams during DADD procedures.

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	No
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
64134	Patient radiation shielding pad/drape, single-use	A protective device intended to be placed on/draped over part of a patient’s body during a diagnostic or therapeutic radiological procedure to shield specific patient anatomies from unnecessary exposure to radiation and/or help block scatter radiation from the patient to protect healthcare workers. It commonly consists of a fluid-resistant outer covering that surrounds a thin sheet of lead (Pb) or lead-equivalent material; it is not a piece of clothing such as an apron. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
KPY	Shield, Protective, Personnel

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 5237c2c3-7ea4-4383-9e32-5a32f326b669
Public Version Date: September 06, 2022
Public Version Number: 1
DI Record Publish Date: August 29, 2022