Procheck

GUDID 00642632018932

MICROLIFE USA, INC.

Intermittent electronic patient thermometer

• Primary Device ID: 00642632018932
• NIH Device Record Key: bd0c5b15-e32a-4ea0-b3c4-85dd310867ca
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Procheck
• Version Model Number: MT16K1-PRO
• Company DUNS: 176387785
• Company Name: MICROLIFE USA, 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00642632018932 [Primary]
GS1	10642632802132 [Package]; Package: Display Box [24 Units]; In Commercial Distribution

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: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-10-24

On-Brand Devices [Procheck]

• 30642632060208: MT16K1-PRO
• 20642632019919: MT18L1-PRO
• 00642632018932: MT16K1-PRO
• 20642632018813: MT19R1-PRO
• 20642632016666: MT1P21-PRO
• 00642632016037: MT16K1-PRO
• 00642632016020: MT16K1-PRO
• 20642632016017: MT16K1BLUE-PRO
• 20642632014440: IR1DY1-1-PRO
• 10642632747006: BP3KV1-5WPC