CONCORD

GUDID 06945040104407

Pulse Oximeter

Contec Medical Systems Co., Ltd.

Pulse oximeter, battery-powered

• Primary Device ID: 06945040104407
• NIH Device Record Key: 34ddf955-3eb2-4a7c-9249-8bfd4d795ea3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CONCORD
• Version Model Number: 85302
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06945040104407 [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: 2018-03-29
• Device Publish Date: 2017-05-05

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