VEGA

GUDID 06946159505024

MT-218

VEGA TECHNOLOGIES INC.

Intermittent electronic patient thermometer

• Primary Device ID: 06946159505024
• NIH Device Record Key: 51c448f6-a272-437a-b551-0995c31e800d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VEGA
• Version Model Number: MT-218
• Company DUNS: 421290561
• Company Name: VEGA TECHNOLOGIES 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	06946159505024 [Primary]
GS1	16946159505021 [Package]; Package: [20 Units]; In Commercial Distribution
GS1	26946159505028 [Package]; Contains: 16946159505021; Package: [10 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: 2
• Public Version Date: 2023-11-13
• Device Publish Date: 2020-06-16

On-Brand Devices [VEGA]

• 06946159501484: CM-01
• 06946159505024: MT-218
• 16946159500217: CM-01