Radius PCG™ 655102

GUDID 07350046132009

Masimo Sweden AB

Patient monitoring system module, carbon dioxide

• Primary Device ID: 07350046132009
• NIH Device Record Key: 6b602eb8-bacf-40f4-a1b7-3eee20472548
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Radius PCG™
• Version Model Number: EMMA Bluetooth mmHg
• Catalog Number: 655102
• Company DUNS: 632369067
• Company Name: Masimo Sweden AB
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07350046132009 [Primary]

FDA Product Code

• CCK: Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-10-27
• Device Publish Date: 2020-10-19

On-Brand Devices [Radius PCG™]

• 07350046132009: EMMA Bluetooth mmHg
• 07350046131996: EMMA Bluetooth kPa