IntiMD

GUDID 06924054300029

Fingertip Pulse Oximeter

SHANGHAI BERRY ELECTRONIC TECH CO., LTD.

Pulse oximeter

• Primary Device ID: 06924054300029
• NIH Device Record Key: 8802c78f-707c-4b0d-90de-c3d8b869900d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IntiMD
• Version Model Number: INT-XM0001
• 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	06924054300029 [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: 2020-05-21

Devices Manufactured by SHANGHAI BERRY ELECTRONIC TECH CO., LTD.

• 06924054300456 - TeleRPM: 2025-01-13 Pulse oximeter
• 06924054300234 - BINACOR: 2023-10-18 Finger pulse oximeter
• 06924054300029 - IntiMD: 2021-11-10Fingertip Pulse Oximeter
• 06924054300029 - IntiMD: 2021-11-10 Fingertip Pulse Oximeter
• 06924054300036 - Aluratek: 2021-11-10 Fingertip Pulse Oximeter
• 06924054300043 - DANAVI: 2021-11-10 Fingertip Pulse Oximeter
• 06924054330163 - NatureSpirit®: 2021-11-10 Fingertip Pulse Oximeter
• 06924054330170 - NatureSpirit®: 2021-11-10 Fingertip Pulse Oximeter
• 06924054300067 - IGUANAMED: 2021-01-29 Fingertip Pulse Oximeter