cofoecare

GUDID 06950715503232

Compression stocking

Cofoe Medical Technology Co.,Ltd

Compression/pressure sock/stocking, reusable

• Primary Device ID: 06950715503232
• NIH Device Record Key: 20f6e5cf-ff78-48fa-a7e6-5dff0088ec10
• Commercial Distribution Discontinuation: 2030-04-27
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: cofoecare
• Version Model Number: KF-WBX-01
• Company DUNS: 544425204
• Company Name: Cofoe Medical 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: 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	06950715503232 [Primary]

FDA Product Code

• DWL: Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)

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: 2024-07-22
• Device Publish Date: 2024-07-12

On-Brand Devices [cofoecare]

• 06950715503263: Compression stocking
• 06950715503256: Compression stocking
• 06950715503249: Compression stocking
• 06950715503232: Compression stocking
• 06950715503225: Compression stocking
• 06950715503218: Compression stocking
• 06950715503201: Compression stocking
• 06950715503195: Compression stocking
• 06950715503188: Compression stocking
• 06950715503171: Compression stocking