PHILIPS IntelliVue MX600 patient monitor 865242

GUDID 00884838029095

Philips Medizin Systeme Böblingen GmbH

Single-patient intensive/general healthcare physiologic monitoring system

• Primary Device ID: 00884838029095
• NIH Device Record Key: 374b7e78-5dd2-4be5-86b7-a910c6dbd162
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PHILIPS IntelliVue MX600 patient monitor
• Version Model Number: 865242
• Catalog Number: 865242
• Company DUNS: 314101143
• Company Name: Philips Medizin Systeme Böblingen GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(999)999-9999
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Device Identifiers

Device Issuing Agency	Device ID
GS1	00884838029095 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K150310

FDA Product Code

• MHX: MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS)

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-02-06
• Device Publish Date: 2016-09-26

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