AMMEX Professional

GUDID 10697383968637

Master Bag

AMMEX CORPORATION

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

• Primary Device ID: 10697383968637
• NIH Device Record Key: d1e03779-216b-4dbf-b8f6-ea27b223d119
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AMMEX Professional
• Version Model Number: ABNPFMP-S
• Company DUNS: 187070768
• Company Name: AMMEX CORPORATION
• 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: false
• Expiration Date: true
• Donation Id Number: false
• 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	10697383968637 [Primary]

FDA Product Code

• LZA: Polymer Patient Examination Glove
• LZC: Medical Glove, Specialty

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: 2023-07-10
• Device Publish Date: 2023-06-30

On-Brand Devices [AMMEX Professional]

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