CONCORD

GUDID 06945040104773

Pulse Oximeter

Contec Medical Systems Co., Ltd.

Pulse oximeter

• Primary Device ID: 06945040104773
• NIH Device Record Key: 84ed7a1f-e75d-407f-8040-71bf67c66dbe
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CONCORD
• Version Model Number: Concord basic CCI-50DL
• Company DUNS: 529606295
• Company Name: Contec Medical Systems Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	06945040104773 [Primary]

FDA Product Code

• OCH: Oximeter, Infrared, Sporting, Aviation

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2021-11-10
• Device Publish Date: 2019-07-30

On-Brand Devices [CONCORD]

• 06945040104407: Pulse Oximeter
• 06945040104391: Pulse Oximeter
• 06945040104384: Pulse Oximeter
• 06945040104377: Pulse Oximeter
• 06945040104360: Pulse Oximeter
• 06945040105657: Pulse Oximeter
• 06945040104773: Pulse Oximeter
• 06945040104766: Pulse Oximeter
• 06945040104759: Pulse Oximeter
• 06945040104742: Pulse Oximeter
• 06945040104735: Pulse Oximeter
• 06945040104728: Pulse Oximeter