Mobile CL 989803165921

GUDID 30884838030900

Philips Medical Systems

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• Primary Device ID: 30884838030900
• NIH Device Record Key: da007b65-5076-43e2-af35-16a4f1fc9034
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mobile CL
• Version Model Number: 989803165921
• Catalog Number: 989803165921
• Company DUNS: 078628040
• Company Name: Philips Medical Systems
• 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: 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

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Device Identifiers

Device Issuing Agency	Device ID
GS1	30884838030900 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K101600

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: 2017-08-14

On-Brand Devices [Mobile CL]

• 00884838030879: 989803165961
• 30884838030900: 989803165921
• 30884838030887: 989803165951
• 30884838020888: 989803165941