AccessGUDID - DEVICE: SJM™ Masters Series Hemashield™ (05414734006507)

GUDID

Device Identifier (DI) Information

Brand Name: SJM™ Masters Series Hemashield™
Version or Model: CAVGJ-514 00
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 29CAVGJ-514 00
Company Name: ST. JUDE MEDICAL, INC.

Primary DI Number: 05414734006507
Issuing Agency: GS1
Commercial Distribution End Date: August 21, 2015
Device Count: 1
Labeler D-U-N-S® Number*: 149818952 *Terms of Use

Device Description: St. Jude Medical Valved Graft Rotatable Mechanical Heart Valve

Device Characteristics

What MRI safety information does the labeling contain?	MR Conditional
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):	Yes
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?
60423	Aortic bi-leaflet mechanical heart valve prosthesis/biologic-polymer aorta graft	An artificial substitute for a natural aortic heart valve fitted with a length of biologic-polymer blood vessel (vascular graft) intended to be implanted during open heart surgery to simultaneously replace a dysfunctional aortic heart valve and repair/replace a damaged or diseased ascending aorta (e.g., in cases of aneurysm, dissection or dilatation). The valve component consists of two flat, semicircular, pyrolytic carbon-coated or polymer leaflets that pivot about struts attached to the valve housing by hinges; the synthetic polymer blood vessel is designed to conform to the aortic root anatomy and is impregnated with a bioabsorbable animal-derived gelatin.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
LWQ	HEART-VALVE, MECHANICAL

FDA Premarket Submission

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

Device Exempt from Premarket Submission: No 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
Special Storage Condition, Specify: Store in cool, dry area until needed.

Clinically Relevant Size

[?]

Size Type Text
Outer Diameter: 29 Millimeter

Device Record Status

Public Device Record Key: 02f56416-32f3-42f6-8ebe-cc7071690257
Public Version Date: February 05, 2021
Public Version Number: 3
DI Record Publish Date: September 23, 2014