Jiekang

GUDID 06975285070014

Zhangjiagang Jiekang Medical Devices Equipment Co.,Ltd.

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• Primary Device ID: 06975285070014
• NIH Device Record Key: 4e884634-5257-4b58-86a2-0888dea2e7f3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Jiekang
• Version Model Number: YJK-F1
• Company DUNS: 542983542
• Company Name: Zhangjiagang Jiekang Medical Devices Equipment 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	06975285070014 [Primary]

FDA Product Code

• FPP: Stretcher, Hand-Carried

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: 2023-02-27
• Device Publish Date: 2023-02-17