Taylor 5732FA

GUDID 06954644457321

Conmo Electronic Co., Ltd

Bioelectrical body composition analyser

• Primary Device ID: 06954644457321
• NIH Device Record Key: 4bda81a2-de5e-42a4-b909-ea7651647051
• Commercial Distribution Discontinuation: 2019-01-01
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Taylor
• Version Model Number: 57324102FB/57324102FT
• Catalog Number: 5732FA
• Company DUNS: 421072579
• Company Name: Conmo Electronic 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: true
• 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	06954644457321 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K140594

FDA Product Code

• MNW: Analyzer, Body Composition

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-01-01
• Device Publish Date: 2016-09-23

On-Brand Devices [Taylor]

• 06954644457802: 578040733FW
• 06954644457710: 57714192F/577141933F
• 06954644457321: 57324102FB/57324102FT