NatureSpirit®

GUDID 06924054330170

Fingertip Pulse Oximeter

SHANGHAI BERRY ELECTRONIC TECH CO., LTD.

Pulse oximeter

• Primary Device ID: 06924054330170
• NIH Device Record Key: 5ca251fc-7219-41b2-b3cc-c3adb4cff42f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NatureSpirit®
• Version Model Number: CP-500E
• Company DUNS: 529404533
• Company Name: SHANGHAI BERRY ELECTRONIC TECH 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	06924054330170 [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: 2020-04-21

On-Brand Devices [NatureSpirit®]

• 06924054330170: Fingertip Pulse Oximeter
• 06924054330163: Fingertip Pulse Oximeter