AccessGUDID - DEVICE: Standard Supreme Surgical Drape Sheet (00634916138566)

GUDID

Device Identifier (DI) Information

Brand Name: Standard Supreme Surgical Drape Sheet
Version or Model: 95500903
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 95500903
Company Name: STANDARD TEXTILE CO., INC.

Primary DI Number: 00634916138566
Issuing Agency: GS1
Commercial Distribution End Date: January 29, 2018
Device Count: 72
Labeler D-U-N-S® Number*: 006999858 *Terms of Use

Device Description: DRAPE SUTURE SHEET 22X22 JADE - 2PLY STANDARD SUPREME W/FEN (SR 14824R)

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: ff4ed368-f602-4c93-8764-c474a2e626a2
Public Version Date: July 06, 2023
Public Version Number: 3
DI Record Publish Date: January 29, 2018