CONCORD CCI-300C3-BLUE-DLX

GUDID 06942820461293

Fingertip Pulse Oximeter

Beijing Choice Electronic Technology Co., Ltd.

Pulse oximeter, battery-powered

• Primary Device ID: 06942820461293
• NIH Device Record Key: 16697c49-6ea9-47fe-b6e1-3be9dca8e98d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CONCORD
• Version Model Number: Concord Sapphire-Deluxe
• Catalog Number: CCI-300C3-BLUE-DLX
• Company DUNS: 526882823
• Company Name: Beijing Choice Electronic Technology Co., Ltd.
• 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: 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	06942820461293 [Primary]

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: 2019-09-19
• Device Publish Date: 2016-10-27

On-Brand Devices [CONCORD]

• 06942820461743: Fingertip Pulse Oximeter
• 06942820461736: Fingertip Pulse Oximeter
• 06942820461729: Fingertip Pulse Oximeter
• 06942820461712: Fingertip Pulse Oximeter
• 06942820461705: Fingertip Pulse Oximeter
• 06942820461699: Fingertip Pulse Oximeter
• 06942820461682: Fingertip Pulse Oximeter
• 06942820461293: Fingertip Pulse Oximeter
• 06942820461286: Fingertip Pulse Oximeter
• 06942820461279: Fingertip Pulse Oximeter
• 06942820461262: Fingertip Pulse Oximeter
• 06942820461255: Fingertip Pulse Oximeter
• 06942820461248: Fingertip Pulse Oximeter
• 06942820461064: Fingertip Pulse Oximeter
• 06942820462061: Concord Fingertip Pluse Oximeter 75059