eox

GUDID 06972167550114

Guangdong Long Yao Electronic Technology Co., Ltd.

Pulse oximeter, line-powered

• Primary Device ID: 06972167550114
• NIH Device Record Key: 1a5cdf6d-48ea-4434-9de6-c5dd74e1cf34
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: eox
• Version Model Number: LYOX01
• Company DUNS: 544492017
• Company Name: Guangdong Long Yao Electronic Technology Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• 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	06972167550114 [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: 2019-04-08
• Device Publish Date: 2019-03-30

Devices Manufactured by Guangdong Long Yao Electronic Technology Co., Ltd.

• 00851950008185 - iOX: 2019-04-25
• 06972167550213 - iox: 2019-04-24
• 06972167550114 - eox: 2019-04-08
• 06972167550114 - eox: 2019-04-08