Geon

GUDID 00084431943686

Digital clinical thermometer

GEON CORPORATION

Intermittent electronic patient thermometer

• Primary Device ID: 00084431943686
• NIH Device Record Key: bb960b07-4d2f-44ff-b81f-ea1620f0142c
• Commercial Distribution Discontinuation: 2021-09-18
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Geon
• Version Model Number: MT-B162A
• Company DUNS: 657229373
• Company Name: GEON CORPORATION
• 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: true
• 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	00084431943686 [Primary]

FDA Product Code

• FLL: Thermometer, Electronic, Clinical

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: 2020-09-29
• Device Publish Date: 2020-09-21