DDU-1XX Pediatric Rescue Pads

GUDID 00815098020430

DEFIBTECH, L.L.C.

External defibrillator electrode, paediatric, single-use External defibrillator electrode, paediatric, single-use External defibrillation electrode, paediatric, single-use External defibrillation electrode, paediatric, single-use External defibrillation electrode, paediatric, single-use External defibrillation electrode, paediatric, single-use External defibrillation electrode, paediatric, single-use External defibrillation electrode, paediatric, single-use External defibrillation electrode, paediatric, single-use External defibrillation electrode, paediatric, single-use External defibrillation electrode, paediatric, single-use External defibrillation electrode, paediatric, single-use External defibrillation electrode, paediatric, single-use External defibrillation electrode, paediatric, single-use External defibrillation electrode, paediatric, single-use External defibrillation electrode, paediatric, single-use External defibrillation electrode, paediatric, single-use

• Primary Device ID: 00815098020430
• NIH Device Record Key: 19cd812d-4e1b-4276-bc4f-07e65a8b8b00
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DDU-1XX Pediatric Rescue Pads
• Version Model Number: DDP-200P
• Company DUNS: 128340200
• Company Name: DEFIBTECH, L.L.C.
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00815098020430 [Primary]
GS1	40815098020438 [Package]; Package: [20 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K033896

FDA Product Code

• MKJ: Automated External Defibrillators (Non-Wearable)

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: 2015-10-24

Devices Manufactured by DEFIBTECH, L.L.C.

• 10815098020437 - DDU-1XX Series Pediatric Pads Configuration: 2023-07-06
• 10815098020451 - DDU-1XXX/2XXX Series Pediatric Pads Configuration: 2023-07-06
• 00815098020737 - DDU-100 Lifeline AED with RX activation form: 2021-08-09 DDU-100 Lifeline AED, US, English, 1 set Adult Pads (DDP-100), Quick Start Card (DAC-501), Op. Guide (DAC-A581-EN), 5 year batte
• 00815098020744 - DDU-100 Lifeline AED with RX activation form: 2021-08-09 DDU-100 Lifeline AED, US, English, 1 set Adult Pads (DDP-100), Quick Start Card (DAC-501), Op. Guide (DAC-A581-EN), 7 year batte
• 00815098020751 - DDU-120 Lifeline AED with RX activation form: 2021-08-09 DDU-120 Lifeline AUTO AED, US, English, 1 set Adult Pads (DDP-100), Quick Start Card (DAC-501), Op. Guide (DAC-A581-EN), 5 year
• 00815098020768 - DDU-120 Lifeline AED with RX activation form: 2021-08-09 DDU-120 Lifeline AUTO AED, US, English, 1 set Adult Pads (DDP-100), Quick Start Card (DAC-501), Op. Guide (DAC-A581-EN), 7 year
• 00815098020775 - DDU-2300 Lifeline VIEW with RX activation form: 2021-08-09 DDU-2300 Lifeline VIEW, US, English, 1 set Adult Pads (DDP-2001), Quick Start Card (DAC-2501), Op. Guide (DAC-A2530EN), 4 year b
• 00815098020782 - DDU-2450 Lifeline ECG with RX activation form: 2021-08-09 DDU-2450 Lifeline ECG, US, English, 1 set Adult Pads (DDP-2001), Quick Start Card (DAC-2501), Op. Guide (DAC-A2530EN), 4 year ba