Stretcher

GUDID 06974679019639

Dragon Medical Co.,Ltd

Hospital stretcher, manual

• Primary Device ID: 06974679019639
• NIH Device Record Key: f8d21a20-a3be-4a00-a53b-6b5b27d2f62b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Stretcher
• Version Model Number: DW-F001
• Company DUNS: 722777218
• Company Name: Dragon Medical 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: 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	06974679019639 [Primary]

FDA Product Code

• FPP: Stretcher, Hand-Carried

Sterilization

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

[06974679019639]

Liquid Chemical

[06974679019639]

Liquid Chemical

[06974679019639]

Liquid Chemical

[06974679019639]

Liquid Chemical

[06974679019639]

Liquid Chemical

[06974679019639]

Liquid Chemical

[06974679019639]

Liquid Chemical

[06974679019639]

Liquid Chemical

[06974679019639]

Liquid Chemical

[06974679019639]

Liquid Chemical

[06974679019639]

Liquid Chemical

[06974679019639]

Liquid Chemical

[06974679019639]

Liquid Chemical

[06974679019639]

Liquid Chemical

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-09-04
• Device Publish Date: 2025-08-27