PHILIPS IntelliVue Pulse Oximetry Module 862112

GUDID 00884838021037

Philips Medizin Systeme Böblingen GmbH

Patient monitoring system module, pulse oximetry

• Primary Device ID: 00884838021037
• NIH Device Record Key: cf7b5128-821e-4004-b41b-0f6c7190e60b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PHILIPS IntelliVue Pulse Oximetry Module
• Version Model Number: 862112
• Catalog Number: 862112
• 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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• Phone: +1(999)999-9999
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• Phone: +1(999)999-9999
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• Phone: +1(999)999-9999
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• Phone: +1(999)999-9999
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• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
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• Phone: +1(999)999-9999
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884838021037 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K150310

FDA Product Code

• DQA: Oximeter

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: 2016-12-28

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