CONCORD

GUDID 06927394500104

Handheld Pulse Oximeter-Rechargeable

Hunan Accurate Bio-Medical Technology Co., Ltd.

Pulse oximeter, battery-powered

• Primary Device ID: 06927394500104
• NIH Device Record Key: 2d825b10-fcd9-493c-8ee3-1e0a9160a5aa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CONCORD
• Version Model Number: 75023R
• Company DUNS: 421349331
• Company Name: Hunan Accurate Bio-Medical Technology Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	06927394500104 [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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-03-22
• Device Publish Date: 2021-03-12

On-Brand Devices [CONCORD]

• 06927394535557: 75023
• 06927394500104: Handheld Pulse Oximeter-Rechargeable
• 06927394500180: Concord Fingertip Pulse Oximeter
• 06927394502474: Concord Wrist Oximeter