VERIDIAN

GUDID 00845717000512

ProKit Aneroid Sphygmomanometer With Dual-Head Scope, Adult, Hunter Green

VERIDIAN HEALTHCARE LLC

Aneroid manual sphygmomanometer

• Primary Device ID: 00845717000512
• NIH Device Record Key: fc044ee1-4b1d-48f3-bf18-58849cacb3d6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VERIDIAN
• Version Model Number: 02-12706
• Company DUNS: 830437997
• Company Name: VERIDIAN HEALTHCARE LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: 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: false

Customer Support Contacts

• Phone: 866-326-1313
• Email: info@veridianhealthcare.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00845717000512 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K082542

FDA Product Code

• DXN: System, Measurement, Blood-Pressure, Non-Invasive

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-26

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