vigorun

GUDID 00818218021072

Famidoc Technology Co.,Ltd.

Infrared patient thermometer, skin

• Primary Device ID: 00818218021072
• NIH Device Record Key: af356909-b2a3-434b-8237-d0f69ebc63ea
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: vigorun
• Version Model Number: FDIR-V4
• Company DUNS: 421343701
• Company Name: Famidoc Technology Co.,Ltd.
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00818218021072 [Primary]

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: 4
• Public Version Date: 2021-08-12
• Device Publish Date: 2019-09-29

On-Brand Devices [vigorun]

• 00854314007381: FDIR-V4
• 08182180241281: FDIR-V4
• 00818218021072: FDIR-V4