AccessGUDID - DEVICE: WATCHMAN® Access System (08714729838210)

GUDID

Device Identifier (DI) Information

Brand Name: WATCHMAN® Access System
Version or Model: M635TU40060
Commercial Distribution Status: In Commercial Distribution
Catalog Number: M635TU40060
Company Name: BOSTON SCIENTIFIC CORPORATION

Primary DI Number: 08714729838210
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 021717889 *Terms of Use

Device Description: Access Sheath with Dilator

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?
45419	Cardiac occluder delivery kit	A collection of devices designed to implant a cardiac occluder (not included) for the non-surgical closure of cardiac defects. The collection may include a delivery catheter/sheath, dilator, loading device, delivery cable, and additional items for the intravascular delivery and deployment of a cardiac occluder. The devices are used in the treatment of cardiac disorders that may include atrial septal defects (ASD), ventricular septal defects (VSD), patent foramen ovale (PFO), or patent ductus arteriosus (PDA). This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
NGV	System, appendage closure, left atrial

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
P130013	000
P130013	005
P130013	008
P130013	017
P130013	019
P130013	025

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
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 3c22180c-e9a4-4b48-8e57-0bf7f86763ef
Public Version Date: February 19, 2021
Public Version Number: 6
DI Record Publish Date: March 20, 2015