Cureguard

GUDID 06938275200389

Jiangsu Cureguard Glove Co., Ltd.

Vinyl examination/treatment glove, non-powdered

• Primary Device ID: 06938275200389
• NIH Device Record Key: bc6ea3c4-7519-4022-af41-c706a3b62220
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cureguard
• Version Model Number: M
• Company DUNS: 527942388
• Company Name: Jiangsu Cureguard Glove Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• 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	06938275200389 [Primary]

FDA Product Code

• LYZ: Vinyl Patient Examination Glove

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: 2021-06-03
• Device Publish Date: 2021-05-26

On-Brand Devices [Cureguard]

• 06938275200365: XS
• 06938275200402: XL
• 06938275200396: L
• 06938275200389: M
• 06938275200372: S