AccessGUDID - DEVICE: Barrier Supreme Surgical Drape (00634916171396)

GUDID

Device Identifier (DI) Information

Brand Name: Barrier Supreme Surgical Drape
Version or Model: 226H1322
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 226H1322
Company Name: STANDARD TEXTILE CO., INC.

Primary DI Number: 00634916171396
Issuing Agency: GS1
Commercial Distribution End Date: December 17, 2024
Device Count: 72
Labeler D-U-N-S® Number*: 006999858 *Terms of Use

Device Description: Small Universal Fenestrated Drape, 1-Ply Barrier Supreme, KAUM 20X20 - RM (98 8155) USE: 22626022

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:	No
Prescription Use (Rx):	No
Over the Counter (OTC):	Yes
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?
47780	Patient surgical drape, reusable	A noninvasive sheet designed to cover a portion of a patient’s anatomy during a surgical procedure to function as a barrier to cross contamination (e.g., isolate a site of surgical incision, protect non-operative anatomy). It is not designed with specific heat-reflective or laser resistant materials. It is available in a variety of designs (e.g., flat sheet with or without an access hole, leg tube). This is a reusable device intended to be sterilized prior to use.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
PUI	Drape, Surgical, Exempt

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: No
Requires Sterilization Prior to Use: Yes

Sterilization Method [?]
Moist Heat or Steam Sterilization

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: 588c4777-c04a-488f-a527-6ea56401c612
Public Version Date: December 30, 2024
Public Version Number: 4
DI Record Publish Date: January 29, 2018