MEIJER 74-362D6

GUDID 10708820121277

Meijer 8-Second Flexible Tip Digital Thermometer

MEIJER, INC.

Intermittent electronic patient thermometer

• Primary Device ID: 10708820121277
• NIH Device Record Key: b1fb9921-d724-4850-9b79-1c34f204cd5c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MEIJER
• Version Model Number: 74-362D6
• Catalog Number: 74-362D6
• Company DUNS: 006959555
• Company Name: MEIJER, INC.
• 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
• Phone: 866-326-1313
• Email: info@veridianhealthcare.com
• Phone: 866-326-1313
• Email: info@veridianhealthcare.com
• Phone: 866-326-1313
• Email: info@veridianhealthcare.com
• Phone: 866-326-1313
• Email: info@veridianhealthcare.com
• Phone: 866-326-1313
• Email: info@veridianhealthcare.com
• Phone: 866-326-1313
• Email: info@veridianhealthcare.com
• Phone: 866-326-1313
• Email: info@veridianhealthcare.com
• Phone: 866-326-1313
• Email: info@veridianhealthcare.com
• Phone: 866-326-1313
• Email: info@veridianhealthcare.com
• Phone: 866-326-1313
• Email: info@veridianhealthcare.com
• Phone: 866-326-1313
• Email: info@veridianhealthcare.com
• Phone: 866-326-1313
• Email: info@veridianhealthcare.com
• Phone: 866-326-1313
• Email: info@veridianhealthcare.com
• Phone: 866-326-1313
• Email: info@veridianhealthcare.com
• Phone: 866-326-1313
• Email: info@veridianhealthcare.com
• Phone: 866-326-1313
• Email: info@veridianhealthcare.com
• Phone: 866-326-1313
• Email: info@veridianhealthcare.com
• Phone: 866-326-1313
• Email: info@veridianhealthcare.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00708820121270 [Primary]
GS1	10708820121277 [Package]; Contains: 30708820121271; Package: Master Carton [72 Units]; In Commercial Distribution
GS1	30708820121271 [Package]; Contains: 00708820121270; Package: Display [6 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K041516

FDA Product Code

• FLL: Thermometer, Electronic, Clinical

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: 2017-05-16

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