Bowflex 57284072FBOW

GUDID 04897077350116

BODY COMPOSITION ANALYZERS

TAYLOR PRECISION PRODUCTS, INC.

Bioelectrical body composition analyser

• Primary Device ID: 04897077350116
• NIH Device Record Key: 856986ce-7168-4528-995f-047b9cf4560e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bowflex
• Version Model Number: 0116
• Catalog Number: 57284072FBOW
• Company DUNS: 036981694
• Company Name: TAYLOR PRECISION PRODUCTS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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	04897077350116 [Primary]

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: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-11-04

Devices Manufactured by TAYLOR PRECISION PRODUCTS, INC.

• 20077784049192 - TAYLOR: 2025-05-14
• 20077784043077 - Taylor: 2022-07-18
• 10077784035402 - Brookstone: 2020-05-06
• 20077784038967 - Taylor: 2020-05-06
• 00077784019740 - Taylor: 2019-11-06
• 40077784018918 - Taylor: 2018-11-05
• 10077784022006 - Taylor: 2018-11-05
• 20077784022652 - Taylor: 2018-11-05