HeartStart 989803210541

GUDID 00884838106642

PHILIPS ELECTRONICS NORTH AMERICA CORPORATION

Internal defibrillator electrode, adult Internal defibrillator electrode, adult Internal defibrillator electrode, adult Internal defibrillator electrode, adult Internal defibrillator electrode, adult Internal defibrillator electrode, adult Internal defibrillator electrode, adult Internal defibrillator electrode, adult Internal defibrillator electrode, adult Internal defibrillator electrode, adult Internal defibrillator electrode, adult Internal defibrillator electrode, adult Internal defibrillator electrode, adult Internal defibrillator electrode, adult Internal defibrillator electrode, adult Internal defibrillator electrode, adult Internal defibrillation electrode, adult, reusable Internal defibrillation electrode, adult, reusable Internal defibrillation electrode, adult, reusable Internal defibrillation electrode, adult, reusable Internal defibrillation electrode, adult, reusable Internal defibrillation electrode, adult, reusable Internal defibrillation electrode, adult, reusable Internal defibrillation electrode, adult, reusable Internal defibrillation electrode, adult, reusable Internal defibrillation electrode, adult, reusable Internal defibrillation electrode, adult, reusable Internal defibrillation electrode, adult, reusable Internal defibrillation electrode, adult, reusable Internal defibrillation electrode, adult, reusable Internal defibrillation electrode, adult, reusable

• Primary Device ID: 00884838106642
• NIH Device Record Key: b5674c6b-e153-45e2-ae2e-671cbb54a647
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HeartStart
• Version Model Number: 989803210541
• Catalog Number: 989803210541
• Company DUNS: 079503890
• Company Name: PHILIPS ELECTRONICS NORTH AMERICA 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: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884838106642 [Primary]

FDA Product Code

• LDD: Dc-defibrillator, low-energy, (including paddles)

Sterilization

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

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

[00884838106642]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-11-08
• Device Publish Date: 2021-10-29

On-Brand Devices [HeartStart]

• 00884838106666: 989803210561
• 00884838106659: 989803210551
• 00884838106642: 989803210541
• 00884838106635: 989803210531
• 00884838111493: HS Adult/Child Radiolucent Pads
• 00884838055728: CPR Compression Meter Adhesive Pads 10-Set