AccessGUDID - DEVICE: CONVERTORS (50885380132283)

GUDID

Device Identifier (DI) Information

Brand Name: CONVERTORS
Version or Model: 49301NS
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 49301NS
Company Name: Cardinal Health 200, LLC

Primary DI Number: 50885380132283
Issuing Agency: GS1
Commercial Distribution End Date: May 04, 2021
Device Count: 14
Labeler D-U-N-S® Number*: 961027315 *Terms of Use

Device Description: Femoral Angiography Drape BNS

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":	Yes
For Single-Use:	Yes
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?
16006	Angiographic drape	A flexible, protective covering made of natural or synthetic materials, or both, designed to be used on patients during an angiographic procedure to control microbial and substance (e.g., blood, contrast material) contamination of the patient entry field. It may be specific for brachial or femoral procedures, and may include a window(s) for viewing and/or a trough to collect spilled substances. This is a single-use device.	Obsolete	false

FDA Product Code

[?]

Product Code	Product Code Name
KKX	Drape, surgical

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 [?]
Ethylene Oxide

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: d7226c9a-e716-4d16-9d73-0db15619e834
Public Version Date: May 04, 2021
Public Version Number: 5
DI Record Publish Date: June 23, 2016