AccessGUDID - DEVICE: PRACTIfilm Barrier Cling Sheets Blue (00723896018163)

GUDID

Device Identifier (DI) Information

Brand Name: PRACTIfilm Barrier Cling Sheets Blue
Version or Model: 704223 4X6 Blue Film
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 704223
Company Name: PRACTICON, INC.

Primary DI Number: 00723896018163
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1200
Labeler D-U-N-S® Number*: 119193803 *Terms of Use

Device Description: Blue PRACTIfilm Barrier Cling Sheets are a simple solution to contamination control. Thinner 1.5 mil polyethylene and special low-tack adhesive give PRACTIfilm the ideal cling quality. Each 4" x 6" sheet sticks anywhere yet removes easily, leaving no residue. 1,200 perforated sheets per roll in a convenient dispenser box.

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?
12535	Medical equipment/instrument drape, single-use	A flexible polymer sheet/bag/sleeve designed to form a protective water-resistant enclosure around a piece of medical equipment/instrument (e.g., C-arm, surgical laser/camera/microscope, examination table/chair) and/or components (e.g., cables, tubes, headrest). It is intended as a hygienic barrier to protect the equipment/instrument from soiling and/or contamination when used inside, or within the vicinity of, a hygienic area; it may have patient contact, however it is not intended to be introduced into a body cavity (noninvasive). It is neither a dedicated handle cover, device cap nor an ultrasound transducer cover. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
PEM	Dental Barriers And Sleeves

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K151123	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
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: 64a79b46-a2e2-408c-b7f1-8857d1929ffc
Public Version Date: September 11, 2024
Public Version Number: 3
DI Record Publish Date: August 14, 2020