REVOSOFT CT

GUDID 09555123602910

NITRILE EXAM POWDER FREE GLOVE SIZE L

CRANBERRY INTERNATIONAL SDN. BHD.

Nitrile examination/treatment glove, non-powdered, non-antimicrobial

• Primary Device ID: 09555123602910
• NIH Device Record Key: e193920b-2391-4100-a3b8-ea010c7f3425
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: REVOSOFT CT
• Version Model Number: 3378
• Company DUNS: 659313067
• Company Name: CRANBERRY INTERNATIONAL SDN. BHD.
• Device Count: 300
• 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: true
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	09555123602910 [Unit of Use]
GS1	09555123608301 [Primary]
GS1	09555123608356 [Package]; Contains: 09555123608301; Package: Case [10 Units]; In Commercial Distribution

FDA Product Code

• LZA: Polymer 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: 2023-09-13
• Device Publish Date: 2023-09-05

On-Brand Devices [REVOSOFT CT]

• 09555123602927: NITRILE EXAM POWDER FREE GLOVE SIZE XL
• 09555123602910: NITRILE EXAM POWDER FREE GLOVE SIZE L
• 09555123602903: NITRILE EXAM POWDER FREE GLOVE SIZE M
• 09555123602897: NITRILE EXAM POWDER FREE GLOVE SIZE S