Fingertip Pulse Oximeter

GUDID 06932562310317

Guangdong Biolight Meditech Co., Ltd.

Pulse oximeter

• Primary Device ID: 06932562310317
• NIH Device Record Key: 972e6ef4-ebcc-4acf-a01d-ef9f8cf8bb6f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Fingertip Pulse Oximeter
• Version Model Number: M50
• Company DUNS: 530120146
• Company Name: Guangdong Biolight Meditech 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: true
• 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	06932562310317 [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: 2019-08-28

On-Brand Devices [ Fingertip Pulse Oximeter]

• 06932562310324: M50L
• 06932562310317: M50