PHILIPS QCPR Meter

GUDID 00884838034648

QCPR METER, BUNDLE ASSY

PHILIPS ELECTRONICS NORTH AMERICA CORPORATION

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• Primary Device ID: 00884838034648
• NIH Device Record Key: eb4125b4-9003-4b87-9bd1-44955c090235
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PHILIPS QCPR Meter
• Version Model Number: 989803149941
• 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884838034648 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K130684

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: 2014-09-24

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