AccessGUDID - DEVICE: THORATEC® HEARTMATE II®, OUTFLOW CANNULA BEND RELIEF, 7.6 CM (3 IN) (00813024010180)

GUDID

Device Identifier (DI) Information

Brand Name: THORATEC® HEARTMATE II®, OUTFLOW CANNULA BEND RELIEF, 7.6 CM (3 IN)
Version or Model: 102781
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 102781
Company Name: Thoratec Corporation

Primary DI Number: 00813024010180
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 070156955 *Terms of Use

Device Description: No description.

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):	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?
61748	Implantable ventricular circulatory assist system outflow cannula, synthetic polymer	An implantable tube intended to function as an outflow for an implantable ventricular circulatory assist system, to channel blood pumped from the left ventricle into the aorta via a surgically-created anastomosis. It is made of a synthetic polymer(s) and does not include biologically-derived materials.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
DSQ	Ventricular (Assisst) Bypass

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
Storage Environment Temperature: between 20 and 30 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 5362542c-48a1-4b87-ac18-5540e285ae43
Public Version Date: February 05, 2021
Public Version Number: 7
DI Record Publish Date: September 20, 2014