R.P.M. PRO

GUDID 00845717011945

R.P.M. PRO Blue Tooth Pulse Oximeter

VERIDIAN HEALTHCARE LLC

Pulse oximeter

• Primary Device ID: 00845717011945
• NIH Device Record Key: 30cc28a8-ff85-4071-90d9-3ae9da4373f4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: R.P.M. PRO
• Version Model Number: 210-3110B
• Company DUNS: 830437997
• Company Name: VERIDIAN HEALTHCARE LLC
• 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: 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00845717011945 [Primary]

FDA Product Code

• PGJ: Oximeter, Wellness

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: 2025-09-16
• Device Publish Date: 2025-09-08

On-Brand Devices [R.P.M. PRO]

• 00845717011938: R.P.M. PRO DIGITAL WEIGHT SCALE , CELLULAR
• 00845717011068: R.P.M. PRO Digital Weight Scale, Bluetooth
• 00845717011945: R.P.M. PRO Blue Tooth Pulse Oximeter
• 00845717011785: R.P.M. PRO WIDE PLATFORM DIGITAL WEIGHT SCALE