Transtek

GUDID 16970729042012

Zhongshan Transtek Electronics Co.,Ltd

Bioelectrical body composition analyser

• Primary Device ID: 16970729042012
• NIH Device Record Key: 6e49ddeb-9a86-4987-8939-615e5aabb62d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Transtek
• Version Model Number: GBF-2008-B1
• Company DUNS: 544411562
• Company Name: Zhongshan Transtek Electronics Co.,Ltd
• 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: false
• Serial Number: true
• 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	16970729042012 [Primary]

FDA Product Code

• PUH: Analyzer, Body Composition, Exempt

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: 2022-06-30
• Device Publish Date: 2022-06-22

On-Brand Devices [Transtek]

• 16970729041008: BS-2001-G1
• 16970729041046: GBS-2104-G
• 16970729041053: GBS-2104-G
• 16970729042012: GBF-2008-B1