Cogent

GUDID 04713157969200

FU SHUN HSING TECHNOLOGY CO., LTD.

Hospital stretcher, manual

• Primary Device ID: 04713157969200
• NIH Device Record Key: 2c296eab-1f08-4a7c-9c66-16d271e16d22
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cogent
• Version Model Number: E920
• Company DUNS: 658779207
• Company Name: FU SHUN HSING TECHNOLOGY 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: true
• 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	04713157969200 [Primary]

FDA Product Code

• FPO: Stretcher, Wheeled

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: 2018-10-22
• Device Publish Date: 2018-09-19

On-Brand Devices [Cogent]

• 04713157969200: E920
• 04713157969002: E900
• 04713157968500: E850
• 04713157966780: E200ix
• 04713157965172: E200i
• 04713157965004: C500
• 04713157963031: ES303
• 04713157963000: E300
• 04713157962263: E200
• 04713157962201: E220
• 04713157961334: E200X