GUDID 00802526067310

Magnet

BOSTON SCIENTIFIC CORPORATION

Cardiac pulse generator test magnet Cardiac pulse generator test magnet Cardiac pulse generator test magnet Cardiac pulse generator test magnet Cardiac pulse generator test magnet Cardiac pulse generator test magnet Cardiac pulse generator test magnet Cardiac pulse generator test magnet Cardiac pulse generator test magnet Cardiac pulse generator test magnet Cardiac pulse generator test magnet Cardiac pulse generator test magnet Cardiac pulse generator test magnet Cardiac pulse generator test magnet Cardiac pulse generator test magnet Cardiac pulse generator test magnet

• Primary Device ID: 00802526067310
• NIH Device Record Key: 5687341b-153f-45dc-857e-3673e73d5dae
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 6860
• Company DUNS: 106295384
• Company Name: BOSTON SCIENTIFIC CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00802526067310 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P830060

FDA Product Code

• LWP: Implantable pulse generator, pacemaker (non-CRT)
• OSR: Pacemaker/icd/crt non-implanted components

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-02-23

Devices Manufactured by BOSTON SCIENTIFIC CORPORATION

• 08714729042549 - Passport: 2024-04-05 Balloon Dilatation Catheter
• 08714729042570 - Passport Kit: 2024-04-05 Balloon Dilatation Catheter Kit
• 08714729042587 - Passport Kit: 2024-04-05 Balloon Dilatation Catheter Kit
• 08714729042594 - Passport Kit: 2024-04-05 Balloon Dilatation Catheter Kit
• 08714729042600 - Passport Kit: 2024-04-05 Balloon Dilatation Catheter Kit
• 08714729154921 - Passport: 2024-04-05 Balloon Dilatation Catheter
• 08714729154969 - Passport: 2024-04-05 Balloon Dilatation Catheter
• 08714729191872 - Passport: 2024-04-05 Balloon Dilatation Catheter