yonker

GUDID 06921745200255

Fingertip Pulse Oximeter

Xuzhou Yongkang Electronic Science Technology Co., Ltd

Pulse oximeter, battery-powered

• Primary Device ID: 06921745200255
• NIH Device Record Key: 2a81437b-1829-442b-8bbd-8b361f2431da
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: yonker
• Version Model Number: YK-81
• Company DUNS: 542753796
• Company Name: Xuzhou Yongkang Electronic Science 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	06921745200255 [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: 2019-01-11
• Device Publish Date: 2018-12-11

On-Brand Devices [yonker]

• 06921745200255: Fingertip Pulse Oximeter
• 06921745200163: Wrist type Blood Pressure Monitor
• 06921745200033: Fingertip Pulse Oximeter
• 06921745200026: Fingertip Pulse Oximeter
• 06921745200156: YK-BPA1